содержание .. 73 74 75 76 ..

Цитогенетика эмбрионального развития - часть 75

Цитогенетика эмбрионального развития человека

582

ultrasound. Report of 66 cases / Daffos F., Capella-Pavlovsky M., Forestier F. // Prenat.

Diagn. — 1983. — Vol. 3, N 4. — P. 271–277.

347. Daniel A. Risk of unbalanced progeny at amniocentesis to carriers of chromosome

rearrangements: data from United States and Canadian Laboratories / Daniel A., Hook E.B.,

Wulf G. // Am. J. Med. Genet. — 1989. — Vol. 31, N 1. — P. 14–53.

348. Davie J.R. Histone modification, chromatin structure, and the nuclear matrix / Davie

J.R. // J. Cell Biochem. — 1996. — Vol. 62, N 2. — Р. 149–157

349. De novo DNA cytosine methyltransferase activities in mouse embryonic stem cells /

Lei H., Oh S.P., Okano M. [et al.] // Development. — 1996. — Vol. 122, N 10. — Р. 3195–

3205.

350. Debrot S. Tetrasomy 16 in the mouse: more sever condition than the corresponding

trisomy / Debrot S., Epstein С. // J. Emrbyol. Exp. Morphol. — 1986. — Vol. 91. — Р. 169–

180.

351. Delineation of DNA replication time zones by fluorescence in situ hybridization /

Selig S. [et al.] // EMBO J. — 1992. — Vol. 11, N 3. — P. 1217–1225.

352. Delozier-Blanchet C.D. B.Trisomy 7 in chorionic villi: follow-up studies of

pregnancy, normal child, and placental clonal anomalies / Delozier-Blanchet C.D., Engel E.,

Extermann P., Pastori B. // Prenat. Diagn. — 1988. — Vol. 8, N 4. — Р. 281–286.

353. Derick-Tan J.S. The significance of alfa-feto-protein (AFP) and human chorionic

gonadotropin (HGC) during first trimester of pregnancy / Derick-Tan J.S., Zehfuss I., Taubert

H.D. // Geburtshilte frauenheilkol. — 1982. — Vol. 42, — N1. — Р. 29–34.

354. Dernburg A.F. Direct evidence of a role for heterochromatin in meiotic chromosome

segregation / Dernburg A.F., Sedat J.W., Hawley R.S. // Cell. — 1996. — Vol. 86, N 1. —

Р. 135–146.

355. Detailed physical map of human chromosomal region 11q12-13 shows high meiotic

recombination rate around the MEN1 locus / Janson M. [et al.] // PNAS. — 1991. — Vol. 88,

N 23. — Р. 10609–10613.

356. Detection of aneuploidy for chromosomes 4, 6, 7, 8, 9, 10, 11, 12, 13, 17, 18, 21, X

and Y by fluorescent in situ hybridization in spermatozoa from nine patients with oligoasthen

oteratozoospermia undergoing intracytoplasmatic sperm injection / Pang M.G. [et al.] // Hum.

Reprod. — 1999. — Vol. 14, N 5. — Р. 1266–1273.

357. Development of the first meiotic prophase stages in human fetal oocytes observed by

light and electron microscopy / Garcia M. [et al.] // Hum. Genet. — 1987. — Vol. 77, N 3. —

P. 223–232.

358. Development of the human dispermic embryo / Sathananthan A.H. [et al.] // Hum.

Reprod. Update. — 1999. — Vol. 5, N 5. — Р. 553–560.

359. Developmental ability of chromosomally abnormal human embryos to develop to the

blastocyst stage / Sandalinas M., Sadowy S., Alikani M. [et al.] // Hum. Reprod. — 2001. —

Vol. 16, N 9. — Р. 1954–1958.

360. Developmental biology and pathology /Eds. A. Gropp, K. Benirschke — Berlin:

Springer-Verlag, 1976. — 185 р.

361. Developmental pattern of gene-specific DNA methylation in the mouse embryo and

germ line / Kafri T. [et al.] // Genes Dev. — 1992. — Vol. 6, N 5. — P. 705–714.

362. Devriendt K. Genetic control of intra-uterine growth / Devriendt K. // Eur. J. Obstet.

Gynecol. Reprod. Biol. — 2000. — Vol. 92, N 1. — Р. 29–34.

363. Differences in DNA methylation during oogenesis and spermatogenesis and their

persistence during early embryogenesis in the mouse / Sanford J.P. [et al.] // Genes and Dev. —

1987. — Vol. 1, N 10. — P. 1039–1046.

364. Dilemma of trisomy 20 mosaicism detected prenatally: is it an innocent finding? /

Reish O. [et al.] // Am. J. Med. Genet. — 1998. — Vol. 77, N 1. — P. 72–75.

365. Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens /

Dork T. [et al.] // Hum. Genet. — 1997. — Vol. 100, N 3–4. — P. 365–377.

583

литература

366. Diverse spermatogenetic defects in human caused by Y chromosome deletions

encompassing a novel RNA-binding protein gene / Reijo R. [et al.] // Nat. Genet. — 1995. —

Vol. 10, N 4. — P. 383–393.

367. DNA base sequence is not the only factor for restriction endonuclease activity on

metaphase chromosomes: evidence using isoschizomeres / Gosalvez J. [et al.] // Cytogenet.

Cell Genet. — 1989. — Vol. 50, N 2–3. — P. 142–144.

368. DNA global hypomethylation in EBV-transformed interphase nuclei / Habib M. [et

al.] // Exp. Cell Res. — 1999. — Vol. 249, N 1. — Р. 46–53.

369. DNA methylation in extraembryonic lineages of mammals / Sanford J.P. [et al.] //

Trends Genet. — 1985. — Vol. 1. — P. 89–93.

370. DNA methylation/histone methylation switch regulates rDNA gene dosage control

and nucleolar dominance / Lawrence R. [et al.] // Mol. Cell. — 2004. — Vol. 13, N 4. —

P. 599–609.

371. DNA replication asynchrony between the paternal and maternal alleles of imprinted

genes does of straddle the R/G transition / Drouin R. [et al.] // Chromosoma. — 1997. —

Vol. 106, N 6. — P. 405–411.

372. Doerfler W. DNA methylation and gene activity / Doerfler W. // Ann. Rev. Biochem. —

1983. — Vol. 52. — Р. 93–124.

373. Down’s syndrome in the male. Reproductive pathology and meiotic studies /

Johannisson R., Gropp A., Winking H., [et al.] // Hum. Genet. — 1983. — Vol. 63, N 2. —

Р. 132–138.

374. Ductus venosus studies in fetuses at high risk for chromosomal or heart abnormalities:

relationship with nuchal translucency measurement and fetal outcome / Bilardo C.M., Muller

M.A., Zikulnig L. [et al.] // Ultrasound Obstet. Gynecol. — 2001. — Vol. 17, N 4. — Р. 288–

294.

375. Dumont M.С. Differential associative behavior of mitotic and meiotic acrocentric

chromosomes / Dumont M.С., Bello M.J., Guichaoua O.L. // Hum. Genet. — 1989. — Vol. 82,

N 1. — P. 35–39.

376. Dupont J.-M. Three year national survey of prenatal cytogenetic activity in France

1998–2000 / Dupont J.-M., Carles E. // E.С.A, Newsletter. — 2004, N 13. — P. 3–8.

377. Dyban A. A cytogenetic study of G1-chromosomes in one-cell stage mouse embryo

and in corresponding second polar body. Evaluation of aneuploidy originated in females

heterozygous for translocation T[14;15]6Ca / Dyban A., Fredine M., Noniashvili E. // Int. J.

Dev. Biol. — 1997. — Vol. 41, N 6. — Р. 859–866.

378. Dyban A. Ocadaic acid induced premature chromosome condensation reflecting the

cell cycle progress in one-cell stage mouse embryos / Dyban A., De Sutter P., Verlinsky Y. //

Mol. Reprod. Dev. — 1993. — Vol. 34, N 4. — Р. 402–415.

379. Dyban A. Preimplantation cytogenetic analysis / Dyban A., De Sutter P., Verlinsky Y.

// Preimplantation diagnosis of genetic diseases: a new technique in assisted reproduction. —

N.-Y.: Wiley-Liss, 1993. — P. 93–127.

380. Dyban A.P., Baranov V.S. Cytogenetics of mammalian embryonic development /

Dyban A.P., Baranov V.S. — Oxford: Сlarendon Press, 1987. — 362 р.

381. Dynamics of DNA replication factories in living cells / Leonhardt H. [et al.] // J. Cell

Biol. — 2000. — Vol. 149, N 2. — P. 271–279.

382. Dystrophin gene analysis and prenatal diagnosis of Duchenne muscular dystrophy in

Russia / Baranov V.S. [et al.] // Prenat. Diagn. — 1993. — Vol. 13, N 5. — Р. 323–333.

383. Early pregnancy / Exalto N. [et al.]. — Mannheim: Boehringer Ingelheim, 1983. —

216 p.

384. Early Prenatal Diagnosis, Fetal Cells and DNA in the Mother. Present State and

Perspectives / Eds. M. Macek, D.W. Bianchi, H. Cuckle — Prague: The Karolinum Press,

2002. — 426 p.

385. Eberl D.F. The role of heterochromatin in the expression of a heterochromatic gene,

Цитогенетика эмбрионального развития человека

584

the rolled locus of Drosophila melanogaster / Eberl D.F., Duyf B.J., Hilliker A.J. // Genetics. —

1993. — Vol. 134, N 1. — Р. 277–292.

386. Edirisinghe W.R. Cytogenetic analysis of human oocytes and embryos in an in-vitro

fertilisation programme / Edirisinghe W.R., Murch A.R., Yovich J.L. // Hum. Reprod. —

1992. — Vol. 7, N 2. — P. 230–236.

387. Edwards R. On the origin and frequency of Y chromosome deletions responsible

for severe male infertility / Edwards R., Bishop С. // Mol. Hum. Reprod. — 1997. — Vol. 3,

N 7. — P. 549–554.

388. Edwards R.G. Oocyte polarity and cell determination in early mammalian embryos /

Edwards R.G., Beard H.B. // Mol. Hum. Reprod. — 1997. — Vol. 3, N 10. — Р. 863–905.

389. Effective priming of neonates born to immune dams against the immunogenic

pseudorabies virus glycoprotein gD by replication-incompetent adenovirus-mediated gene transfer

at birth / Monteil M. [et al.] // J. Gen. Virol. — 1997. — Vol. 78, N 12. — Р. 3303–3310.

390. Effects of cadmium on DNA-(Cytosine-5) methyltransferase activity and DNA

methylation status during cadmium-induced cellular transformation /Takiguchi M., Achanzar

W.E., Qu W. [et al.] // Exp. Cell Res. — 2003. — Vol. 286, N 2. — Р. 355–365.

391. Efficient direct chromosome analysis and enzyme determinations from chorionic villi

sampling in the first trimester of pregnancy / Simoni G. [et al.] // Hum. Genet. — 1983. —

Vol. 63, N 4. — P. 349–357.

392. Ehrlich M. DNA methylation: normal development, inhereired diseases and cancer /

Ehrlich M. // J. Clin. Ligand Assay. — 2000. — Vol. 23. — P. 144–146.

393. Eichenhlaub-Ritter U. Alterations in the microtubular cytoskeleton and increased

disorder of chromosome alignment in spontaneously ovulated mouse oocytes aged in vivo:

An immunofluorescent study / Eichenhlaub-Ritter U., Chandley A.С., Gosden R.G. //

Chromosoma. — 1986. — Vol. 94, N 5. — Р. 337–345.

394. Eichenhlaub-Ritter U. Nondisjunction, disturbances in spindle structure, and

characteristics of chromosome alignment in mature oocytes in mice heterozygous for

Robertsonian translocations / Eichenhlaub-Ritter U., Winking H. // Cytogenet. Cell Genet. —

1990. — Vol. 54, N 1–2. — P. 47–54.

395. Eichenlaub-Ritter U. Genetics of oocyte aging / Eichenlaub-Ritter U. // Maturitas. —

1998. — Vol. 30, N 2. — Р. 143–169.

396. Eichenlaub-Ritter U. Mechanisms of nondisjunction in mammalian meiosis /

Eichenlaub-Ritter U. // Curr. Top. Devel. Biol. — 1994. — Vol. 29. — P. 281–324.

397. Electron microscopy and biochemical analysis of mouse metaphase chromosomes

after digestion with restriction endonucleases / Gosalvez J. [et al.] // Chromosoma. — 1990. —

Vol. 99, N 1. — P. 36–43.

398. Elgin S.С.R. Heterochromatin: Silence is golden / Elgin S.С.R., Grewal Sh.I.S. //

Current Biol. — 2004. — Vol. 13, N 23. — Р. 895–898.

399. Elledge S.J. Cell cycle chekpoints: preventing an identity crisis / Elledge S.J. //

Science. — 1996. — Vol. 274, N 5293. — Р. 1664–1672.

400. Ellison J. PHOG, a candidate gene for involvement in the short stature of Turner

syndrome / Ellison J., Wardak Z., Young M. // Hum. Mol. Genet. — 1997. — Vol. 6, N 8. —

Р. 1341–1347.

401. Elucidation the mechanisms of paternal non-disjunction of chromosome 21 in

humans / Savage A.R. [et al.] // Hum. Mol. Genet. — 1998. — Vol. 7, N 8. — Р. 1221–1227.

402. Engel E. Genomic imprinting and uniparental disomy in medicine:clinical and

molecular aspects / Engel E., Antonarakis S.E. — N.-Y.: Wiley-Liss Inc., 2002. — 304 p.

403. Engel E. Imprinting is also a mechanism for immediate or delayed hemizygous

expression of several uniparental haplotypes selected from the genome of each sex / Engel E. //

Am. J. Med. Genet. — 1997. — Vol. 70, N 1. — Р. 95–98.

404. Epigenotype switching of imprintable loci in embryonic germ cells / Tada T. [et al.]

// Dev. Genes Evol. — 1998. — Vol. 207, N 8. — Р. 551–561.

585

литература

405. Epner E. Asynchronous DNA replication within the human β-globin gene locus /

Epner E., Forrester W.С., Groudine M. // PNAS. — 1988. — Vol. 85, N 21. — P. 8081–8085.

406. ESHRE PGD Consortium: Preliminary assesement of data from January 1997 to

September 1998 // Hum. Reprod. — 1999. — Vol. 14, N 12. — Р. 3138–3148.

407. Estimate of aneuploidy using multicolor fluorescence in situ hybridization on human

sperm / Bischoff F.Z., Nguyen D.D., Burt K.J. [et аl.] // Cytogenet. Cell Genet. — 1994. —

Vol. 66, N 4. — P. 237–243.

408. EUCROMIC: Quality Guidelines and standards for Genetic laboratories/clinics in

prenatal diagnosis on fetal samples obtained by invasive procedures // Eur. J. Hum. Genet. —

1998. — Vol. 5, N 6. — Р. 342–350.

409. Evaluation of cytogenetic analysis for clinical preimplantation diagnosis / Santalo J.

[et al.] // Fertil. Steril. — 1995. — Vol. 64, N 1. — P. 44–50.

410. Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1 / Zinn A.R. [et al.] //

Am. J. Hum. Genet. — 1998. — Vol. 63, N 6. — P. 1757–1766.

411. Evidence for increased prevalence of SRY mutations in XY females with complete

rather than partial gonadal dysgenesis / Hawkins J.R. [et al.] // Am J. Hum. Genet. — 1992. —

Vol. 51, N 5. — Р. 979–984.

412. Evidence for methylation of inactive human rRNA genes in amplified regions /

Tantravahi U. [et al.] // Hum. Genet. — 1981. — Vol. 56, N 3. — P. 315–320.

413. Evidence from Turners syndrome of an imprinted X-linked locus affecting cognitive

function / Skuse D. [et al.] // Nature. — 1997. — Vol. 387, N 6634. — P. 705–708.

414. Evsikov S. Mosaicism in inner cell mass of human blastocysts / Evsikov S., Verlinsky

Y. // Hum. Reprod. — 1998. — Vol. 13, N 11. — Р. 3151–3155.

415. Evsikov S.V. Preimplantation development of manipulated mouse zygotes fused with

the second polar bodies: a cytogenetic study / Evsikov S.V., Evsikov A.V. // Int. J. Dev. Biol. —

1994. — Vol. 38, N 4. — Р. 725–730.

416. Expression of an exogenous eukaryotic DNA methyltransferase gene induces

transformation of NIH 3T3 cells / Wu J., Issa J.P., Herman J. [et al.] // PNАS. — 1993. —

Vol. 90, N 19. — P. 8891–8895.

417. Expression of RBM in the nuclei of human germ cells is dependent on a critical

region of the Y chromosome long arm / Elliot D. [et al.] // PNAS. — 1997. — Vol. 94, N 8. —

P. 3848–3853.

418. Expression of Xist during mouse development suggests a role in the initiation of X

chromosome inactivation / Kay G.F., Penny G.D., Patel D. [et al.] // Cell. — 1993. — Vol. 72,

N 2. — Р. 171–182.

419. Farber R.A. Differences in the order of termination of DNA replication in human

chromosomes in peripheral blood lymphocytes and skin fibroblasts from the same individual /

Farber R.A., Davidson R.L. // Cytogenet. Cell Genet. — 1977. — Vol. 18, N 6. — P. 349–

363.

420. Fedorova I. FISH analysis of aneuploidy in spermatozoa / Fedorova I., Loginova Y.,

Kuznetzova T. // Cytogen. Cell Genet. — 1999. — Vol. 77, N 1–2. — P. 61.

421. Feigelson J. Anomalies du sperme, des deferents et de l’epididyme dans la

mucoviscidose / Feigelson J., Pecau Y. // La Presse Medicale. — 1986. — Vol. 15, N 11. —

P. 523–525.

422. Ferraro M. Differential gene activity visualized on sister replication in the presance of 5-

azacytidine / Ferraro M., Lavia P. // Chromosoma. — 1985. — Vol. 91, N 3–4. — P. 307–312

423. Fertility and pregnancy outcome in Danish women with Turner syndrome / Birkebaek

N.H. [et al.] // Clin. Genet. — 2002. — Vol. 61. — P. 35–39.

424. Fetal sex prediction by sex chromatin of chorion villi cells during pregnancy // Chin.

Med. J. — 1975. — Vol. 1, N 2. — P. 117–126.

425. First meiotic division abnormalities in human oocytes: mechanism of trisomy formation /

Angell R.R. [et al.] // Cytogenet. Cell Genet. — 1994. — Vol. 65, N 3. — Р. 194–202.

Цитогенетика эмбрионального развития человека

586

426. First trimester amniofiltration: technical, cytogenetic and pregnancy outcome of 104

consecutive procedures / Burne D.L. [et al.] // Br. J. Obstetr. Gynecol. — 1995. — Vol. 102. —

Р. 220–223.

427. First trimester fetal diagnosis of genetic disorders: clinical evaluation of 250

cases / Brambati B. [et al.] // J. Med. Genet. — 1985. — Vol. 22, N 2. — P. 92–99.

428. First trimester prenatal diagnosis using endocervical lavage: a negative

evaluation / Goldberg M.F. [et al.] // Am. J. Obstetr. Gynecol. — 1980. — Vol. 138,

N 4. — Р. 436–439

429. FISH-deletion mapping defines a 270-kb short stature critical interval in the

pseudoautosomal region PAR1 on human sex chromosomes / Rao E. [et al.] // Hum.

Gen. — 1997. — Vol. 100, N 2. — Р. 236–239.

430. Flake A.W. In utero stem cell transplantation / Flake A.W. // Best. Pract. Res.

Clin. Obstet. Gynecol. — 2004. — Vol. 18, N 6. — P. 941–958.

431. Fluorescence in situ hybridisation analysis and ovarian histology of women

with Turner syndrome presenting with Y-chromosomal material: a correlation between

oral epithelial cells, lymphocytes and ovarian tissue / Hanson L. [et al.] // Hereditas. —

2002. — Vol. 137, N 1. — P. 1–6.

432. Ford С.E. Mosaicism and chimeras / Ford С.E. // Br. Med. Bull. — 1969. —

Vol. 25. — P. 104–109.

433. Forty-four probands with an additional marker chromosome / Buckton K.E. [et

al.] // Hum. Genet. — 1985. — Vol. 69, N 4. — P. 353–370.

434. Foudila T. Turner’s syndrome and pregnancies after oocyte donation / Foudila T.,

Soderstrom-Anttila V., Hovatta O. // Hum. Reprod. — 1999. — Vol. 14, N 2. — P. 532–

535.

435. Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma /

Greger V. [et al.] // Hum. Genet. — 1994. — Vol. 94, N 5. — P. 491–496.

436. Functional interrelationships between nuclear structure and transcriptional

control: contribution to regulation of cell-cycle — and tissue specific gene expression /

Stein G.S. [et al.] // J. Cell. Biochem. — 1996. — Vol. 62, N 2. — Р. 198–209.

437. Gabriel-Robez O. The meiotic pairing behaviour in human spermatocytes carrier

of chromosome anomalies and their repercussions on reproductive fitness / Gabriel-Robez

O., Rumbler Y. // Ann. Genet. — 1994. — Vol. 37, N 1. — P. 3–10.

438. Gap junctional communication during human trophoblast differentiation:

influence of human chorionic gonadotropin / Cronier L. [et al.] // Endocrinol. — 1994. —

Vol. 135, N 1. — P. 402–408.

439. Gebrane-Younes J. When rDNA transcription is arrested during mitosis, UBF is

still associated with non-condensed rDNA / Gebrane-Younes J., Fomproix N., Hernandez-

Verdun D. // J. Cell Sci. — 1997. — Vol. 110., Pt. 19. — Р. 2429–2440.

440. Genetic analysis of mosaicism in 53 women with Turner syndrome / Hanson L.

[et al.] // Hereditas. — 2001. — Vol. 134, N 2. — P. 153–159.

441. Genetic evidence equating SRY and the testis-determining factor / Berta P.,

Hawkins J.R., Sinclair A.H. [et al.] // Nature. — 1990. — Vol. 348, N 6300. — Р. 448–

450.

442. Gilles С.B. The pachytene synaptonemal complex complement of the cat / Gilles

С.B., Cowan S.K. // Genetica. — 1985. — Vol. 67. — Р. 99–107.

443. Girardi S. Submicroscopic deletions in the Y chromosome of infertile men /

Girardi S., Mielnik A., Schlegel P. // Hum. Reprod. — 1997. — Vol. 12, N 8. — P. 1635–

1641.

444. Golubovsky M.D. Oocytes physically and genetically link three generations:

genetic/demographic implications / Golubovsky M.D., Manton K. // Environment and

Human Health: Materials of International Ecological Forum, 27–29 July, 2003. — St.-

Petersburg, 2003. — P. 354-356.

587

литература

445. Golubovsky M.D. Postzygotic diploidization of triplids as a source of unusual

cases of mosaicism,chimerism and twinning / Golubovsky M.D. // Hum. Reprod. —

2003. — Vol. 18, N 2. — Р. 236–242.

446. Gonzales I. Complete sequence of the 43-Kb human ribosomal DNA repeat: analysis

of the intergenic spacer / Gonzales I., Sylvester J. // Cytogenet. Cell Genet. — 1991. — Vol. 57,

N 4. — P. 175–178.

447. Goto T. Expression of an Xist promoter-luciferase construct during spermatogenesis

and in preimplantation embryos: regulation by DNA methylation / Goto T., Christians E.,

Monk M. // Mol. Reprod. Dev. — 1998. — Vol. 49, N 4. — Р. 356–367.

448. Goto T. Regulation of X-chromosome inactivation in development in mice and

human / Goto T., Monk M. // Microbiol. Mol. Biol. Rev. — 1998. — Vol. 62, N 2. — Р. 362–

378.

449. Griffin D.K. The incidence, origin and etiology of aneuploidy / Griffin D.K. // Int.

Rev. Cytol. — 1996. — Vol. 167. — P. 263–295.

450. Guillen A.K. Transcriptional repression mechanisms of nucleolus organizer regions

(NORs) in humans and chimpanzees / Guillen A.K., Hirai Y., Tanoue T., Hirai H. // Chromosome

Res. — 2004. — Vol. 12, N 3. — Р. 225–237.

451. Guttenbach M. Analysis of structural and numerical chromosome abnormalities

in sperm of normal men and carriers of constitutional chromosome aberration. A review /

Guttenbach M., Engel W., Schmid M // Hum. Genet. — 1997. — Vol. 100, N 1. — Р. 1–21.

452. Hahnemann J.M. Accuracy of cytogenetic findings on chorionic villus sampling

(CVS) — diagnodtic consequences of CVS mosaicism and non-mosaic discrepancy in centres

contributing to EUCROMIC 1986–1992 / Hahnemann J.M., Vejerslev L.O. // Prenat. Diagn. —

1997. — Vol. 17, N 9. — Р. 801–817.

453. Hahnemann N. Chromosome studies in induced abortions / Hahnemann N. // Clin.

Genet. — 1973. — Vol. 4, N 4. — Р. 328–332.

454. Hahnemann N. Early prenatal diagnosis: A study of biopsy techniques and cell

culturing from extra-embryonic membrane / Hahnemann N. // Clin. Genet. — 1974. — Vol. 6,

N 4. — Р. 294–306.

455. Handyside A.H. Preimplantation genetic diagnosis: strategies and surprises /

Handyside A.H., Delhanty J.D.A. // TIG. — 1997. — Vol. 13, N 7. — Р. 270–275.

456. Hardy K. The human blastocyst: cell number, death and allocation during late

preimplantation development in vitro / Hardy K., Handyside A.H., Winston R.M.L. //

Development. — 1989. — Vol. 107, N 3. — Р. 597–604.

457. Hassold T. To err (meiotically) is human: the genesis of human aneuploidy / Hassold

T., Hunt P. // Nat. Rev. Genet. — 2001. — Vol. 2, N 4. — P. 280–291.

458. Hassold T. Down syndrome: genetic recombination and the origin of the extra chromosome

21 / Hassold T., Sherman S. // Clin. Genet. — 2000. — Vol. 57, N 2. — P. 95–100.

459. Hassold T. The origin of human nondisjunction: two hits to trisomy / Hassold T. //

Cytogenet. Cell Genet. — 1999. — Vol. 85, N 1–2. — P. 7.

460. Hassold T. Counting cross-overs: characterizing meiotic recombination in mammals /

Hassold T., Sherman S., Hunt P. // Hum. Mol. Genet. — 2000. — Vol. 9, N 16. — Р. 2409–

2419.

461. Hawley R.S. Separation anxiety: the etiology of nondisjunction in files and people /

Hawley R.S., Frazier J.A., Rasooly R. // Hum. Mol. Genet. — 1994. — Vol. 3, N 9. — Р. 1521–

1528.

462. Hecht F. The nonrandomness of human chromosome abnormalities / Hecht F. //

Population Cytogenetics. Studies in humans / Eds. E.B. Hook, I.N. Porter. — N.-Y., London:

Academic Press, 1977. — P. 237–250.

463. Henderson A. Location of ribosomal DNA in human chromosome complement /

Henderson A., Warburton D., Atwood K. // PNAS. — 1972. — Vol. 69, N 11. — P. 3394–

3398.

Цитогенетика эмбрионального развития человека

588

464. Henderson A. Satellite-association frequency and rDNA content of a double-satellited

chromosome / Henderson A., Atwood K. // Hum. Genet. — 1976. — Vol. 31, N 1. — P. 113–115.

465. Henderson S.A. Chiasms frequency and maternal age in mammals / Henderson S.A.,

Edwards R.G. // Nature. — 1968. — Vol. 218, N 136. — Р. 22–28.

466. Hendrich B. Identification and characterization of a family of mammalian methyl-

CpG-binding proteins / Hendrich B., Bird A. // Mol. Cell Biol. — 1998. — Vol. 18, N 11. —

P. 6538–6547.

467. Hendrich B. Mammalian methyltransferases and methyl-CpG-binding domains:

proteins involved in DNA methylation / Hendrich B., Bird A. // Curr. Top Microbiol.

Immunol. — 2000. — Vol. 249. — P. 55–74.

468. Hertig A.T. A description of 34 human ova within the first 17 days of development /

Hertig A.T., Rock J., Adams E.С. // Am. J. Anat. — 1956. — Vol. 98, N 3. — P. 435–459.

469. Heyting С. Synaptonemal complexes: structure and function / Heyting С. // Curr.

Opin. Cell. Biol. — 1996. — Vol. 8, N 3. — Р. 389–396.

470. High frequency of well-defined Y-chromosomal deletions in idiopathic Sertoli cell-

only syndrome / Foresta С. [et al.] // Hum. Reprod. — 1998. — Vol. 13, N 2. — P. 302–307.

471. Hirahara F. A case of tracheal agenesis delivered in patient with mosaic Turners

syndrome / Hirahara F., Miyagi E., Yamanaka M. // Eur. J. Obstet. Gynecol. Reprod. Biol. —

1995. — Vol. 58, N 2. — Р. 207–209.

472. Hodgson С. P. The vector void in gene therapy / Hodgson С. P. // Biotechnology. —

1995. — Vol. 13, N 3. — Р. 222–225.

473. Holmquist G.P. Chromosome bands, their chromatin flavours and their functional

features / Holmquist G.P. // Am. J. Hum. Genet. — 1992. — Vol. 51, N 1. — P. 17–37.

474. Holmquist G.P. Role of replication time in the control of tissue-specific gene

expression / Holmquist G.P. // Am. J. Hum. Genet. — 1987. — Vol. 40, N 2. — P. 151–173.

475. Holms J.M. Aneuploidy detection in human sperm nuclei using fluorescence in situ

hybridization / Holms J.M., Martin K.H. // Hum. Genet. — 1993. — Vol. 91, N 1. — P. 20–

24.

476. Holsclaw D.S. Genital abnormalities in male patients with cystic fibrosis / Holsclaw

D.S., Perlmutter A.D., Jockin H., Shwachman H.H. // J. Urol. — 1971. — Vol. 106, N 4. —

P. 568–574.

477. Holzgreve W. Prenatal karyotyping: when, whom and how? / Holzgreve W., Terzanli

S., Schneider H.P. G., Miny P. // Ultrasound Obstetr. Gynecol. — 1992. — Vol. 2, N 1. —

P. 64–69.

478. Holzgreve W. Enrichment of fetal cells and free fetal DNA from maternal blood: An

insight into the Basel experience / Holzgreve W., Zhong X.Y., Burk M.R., Hahn S. // Early

Pregnancy. — 2001. — Vol. 5, N 1. — P. 43–44.

479. Hook E., Warburton D. The distribution of chromosomal genotypes associated with

Turners syndrome: live birth prevalence rates & evidence for diminished fetal mortality and

severity in genotypes associated with structural X abnormalities of mosaicism / Hook E.,

Warburton D. // Hum. Genet. — 1983. — Vol. 64, N 1. — P. 24–27.

480. Howell W.M. Controlled silver staining of nucleolus organizer regions with a

protective colloid developeer: a one step method / Howell W.M., Black D.A. // Experientia. —

1980. — Vol. 36, N 8. — P. 10–14.

481. Howlett S.K. Methylation levels of maternal and paternal genomes during preim-

plantation development / Howlett S.K., Reik W. // Development. — 1991. — Vol. 113, N 1. —

Р. 19–27.

482. Hsu L.Y.F. Prenatal diagnosis of chromosomal abnormalities through amniocentesis /

Hsu L.Y.F. // Genetic disorders and the fetus. Diagnosis, prevention, and treatment / Ed.

А. Milunsky — Baltimore: The John Hopkins Univ. Press, 1992. — P. 155–210.

483. Hsu T.С. Human and mammalian cytogenetics / Hsu T.С. — N.-Y.: Springer-Verlag,

1979. — 186 p.

589

литература

484. Hulten M. Low chiasmata count and other meiotic irregularities in two infertile

46,XY men with spermatogenic arrest / Hulten M., Eliassоn R., Tillinger K.G. // Hereditas. —

1970. — Vol. 65, N 2. — Р. 285–290.

485. Human centromeric DNAs / Lee С. [et al.] // Hum. Genet. — 1997. — Vol. 100,

N 3–4. — P. 291–304.

486. Human male infertility and Y chromosome deletions: role of the AZF-candidate

genes DAZ, RBM and DFFRY / Ferlin A. [et al.] // Hum. Reprod. — 1999. — Vol. 14, N 7. —

P. 1710–1716.

487. Human male infertility: chromosome anomalies, meiotic disorders, abnormal

spermatozoa and recurrent abortion / Egozcue S. [et al.] // Hum. Repr. Update. — 2000. —

Vol. 6, N 1. — Р. 93–105.

488. Human Y chromosome azoospermia factors (AZF) mapped to different subregions in

Y q11 / Vogt P.H. [et al.] // Hum. Mol. Genet. — 1996. — Vol. 5, N 7. — P. 933–943.

489. Hunt P. A. The control of mammalian female meiosis: factors that influence

chromosome segregation / Hunt P. A. // J. Assist. Reprod. Genet. — 1997. — Vol. 15, N 2. —

Р. 246–252.

490. Hurt E. Nucleus and gene expression. Nuclear compartments and nuclear machines /

Hurt E., Schutz G. // Curr. Opin in Cell Biol. — 1998. — Vol. 10, N 3. — Р. 301–303

491. Hyett T.T. Increased nuchal translucency in trisomy 21 fetues: relations to narrowing

of the aortic isthmus / Hyett T.T., Moscoso G., Nicolaides R. // Hum. Reprod. — 1995. —

Vol. 10, N 11. — Р. 3049–3051.

492. Hypomethylation of classical satellite DNA and chromosome instability in

lymphoblastoid cell lines / Almeida A. [et al.] // Hum. Genet. — 1993. — Vol. 91, N 6. —

P. 538–546.

493. Hypomethylation of human sperm pronuclear chromosomes / Martorell M.R., Navarro J.,

Marquez C.[et al.] // Cytogen. Cell Genet. — 1997. — Vol. 76, N 3–4. — Р. 123–127.

494. Hypomethylation of pericentromeric DNA in breast adenocarcinomas / Narayan A., Ji

W., Zhang X.Y., Marrogi A. [et al.] // Int. J. Cancer — 1998. — Vol. 77, N 6. — P. 833–838.

495. Identification of chromosomal bands replicating early in the S phase of normal

human fibroblasts / Cohen S.M. [et al.] // Exp. Cell Research. — 1998. — Vol. 245, N 2. —

P. 321–329.

496. Identification of the gene-richest bands in human chromosomes / Saccone S. [et al.]

// Gene. — 1996. — Vol. 174, N 1. — P. 85–94.

497. IHGSC (International Human Genome Sequencing Consortium) Initial sequencing

analysis of the human genome // Nature. — 2001. — Vol. 409. — P. 860–921.

498. Illmensee K. Cloning in reproductive medicine / Illmensee K. // J. Assist. Reprod.

Genet. — 2000. — Vol. 18, N 8. — Р. 451–467.

499. Immunolocalization of α-tubulin, γ-tubulin and CENP-E in male Rat and male mouse

meiotic divisions: pathway of meiosis I spindle formation in mammalian spermatocytes / Kallio

M. [et al.] // Devel. Biol. — 1998. — Vol. 195, N 1. — Р. 29–37.

500. Imprinted expression of the Igf2r gene depends on an intronic CpG island / Wutz A.,

Smrzka O.W., Schweifer N. [et al.] // Nature. — 1997. — Vol. 389, N 6652. — P. 745–749.

501. In situ nick-translation distinguishes between active and inactive X chromosomes /

Kerem B.S. [et al.] // Nature. — 1983. — Vol. 304, N 5921. — P. 88–90.

502. Incidence of diploid and disomic sperm sperm nuclei in 45 infertile men / Guttenbach

M. [et al.] // Hum. Reprod. — 1997. — Vol. 12, N 3. — Р. 468–472.

503. Increased incidence of disomic sperm nuclei in a 47,XXY male assessed by

fluorescence in situ hybridization (FISH) / Blanco J. [et al.] // Hum Genet. — 1997. — Vol. 99,

N 3. — Р. 413–416.

504. Increased risk of Alzheimer’s disease in mothers of adults with Down’s syndrome /

Schupf N. [et al.] // Lancet. — 1994. — Vol. 344, N 8919. — P. 353–356.

505. Inheritance of ribosomal gene activity and level of DNA methylation of individual

содержание .. 73 74 75 76 ..