Chromosome polymorphism in 110 couples with reproductive failure and subsequent pregnancy outcome

Fertility and Sterility

Volumn 38, Issue 6, 1982, Pages 688-694

  Tho, S P T ^a   Byrd, J R ^a   McDonough, P G ^a  

^a MEDICAL COLLEGE OF GEORGIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; BIRTH DEFECT; CHROMOSOME INVERSION 16; CHROMOSOME INVERSION 9; CHROMOSOME POLYMORPHISM; CHROMOSOME TRANSLOCATION; CHROMOSOME VARIANT; CONGENITAL DISORDER; CONGENITAL MALFORMATION; DIAGNOSIS; ETIOLOGY; FEMALE GENITAL SYSTEM; FETUS; HEREDITY; HISTOLOGY; HUMAN; IN VITRO STUDY; INFERTILITY; MAJOR CLINICAL STUDY; PREGNANCY; PROGENY; SPONTANEOUS ABORTION;

EID: 0020405366     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0015-0282(16)46695-1     Document Type: Article

References (23)

1. M. Seabright The use of proteolytic enzymes for the mapping of structural rearrangements in the chromosomes of man Chromosoma 36 1972 204
2. T. Caspersson L. Zech C. Johansson Analysis of human metaphase chromosome set by aid of DNA-binding fluorescent agents Exp Cell Res 62 1970 490
3. F.E. Arrighi T.C. Hsu Localization of heterochromatin in human chromosomes Cytogenet Cell Genet (continues Cytogenetics) 10 1971 81
4. C. Goodpasture S.E. Bloom Visualization of nuclear organizer regions in mammalian chromosomes using silver staining Chromosoma 53 1975 37
5. Paris Conference, 1971: Standardization in human cytogenetics Birth Defects: Original Articles Series, VIII 1972 The National Foundation New York 7
6. Paris Conference, 1971: Standardization in human cytogenetics (Suppl) Birth Defects: Original Articles Series, XI 1975 The National Foundation New York 9
7. J. Nielsen U. Friedrich A.B. Hreidarsson E. Zeuthen Frequency of 9qh + and risk of chromosome aberrations in the progeny of individuals with 9qh + Hum Genet (continues Humangenetik) 21 1974 211
8. C.E. Bott G.S. Sekhon H.A. Lubs Unexpectedly high frequency of paternal origin of trisomy 21. (Abstr) Am J Hum Genet 27 1975 20A
9. J. Boué J.L. Taillermite L.C. Hazael-Massieux A. Boué Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families Hum Genet (continues Humangenetik) 30 1975 217
10. P.A. Jacobs A. Frackiewicz P. Law C.J. Hilditch N.E. Morton The effect of structural aberrations of the chromosomes on reproductive fitness in man. II. Results Clin Genet 8 1975 169
11. C. Tsenghi C. Metaxotou-Stavridaki M. Stratakibenetou A. Kalpini-Mavrou N. Matsaniotis Chromosome studies in couples with repeated spontaneous abortions Obstet Gynecol 47 1976 463
12. W.M. Court-Brown Chromosome studies on the general population In Human Population Cytogenetics 1967 North Holland Publishing Co. Amsterdam 1
13. S.R. Patil H.A. Lubs A possible association of long Y chromosomes and fetal loss Hum Genet (continues Humangenetik) 35 1977 233
14. J. Nielsen Large Y chromosome (Yq +) and increased risk of abortion Clin Genet 13 1978 415
15. P. Genest Chromosome variants and abnormalities detected in 51 married couples with repeated abortions Clin Genet 16 1979 387
16. Z. Papp S. Gardo B. Dolhay Chromosome study of couples with repeated spontaneous abortions Fertil Steril 25 1974 713
17. B.E. Ward G.P. Henry A. Robinson Cytogenetic studies in 100 couples with recurrent spontaneous abortions Am J Hum Genet 32 1980 549
18. C. Stoll Cytogenetic findings in 122 couples with recurrent abortions Hum Genet (continues Humangenetik) 57 1981 101
19. A. De La Chapelle J. Schröder K. Stenstrand J. Fellman R. Herba M. Saarni I. Anttolainen I. Tallila L. Tervilä L. Husa G. Tallqvist E.B. Robson P.J.L. Cook R. Sanger Pericentric inversions of human chromosomes 9 and 10 Am J Hum Genet 26 1974 746
20. J.R. Byrd D.E. Askew P.G. McDonough Cytogenetic findings in fifty-five couples With recurrent fetal wastage Fertil Steril 28 1977 246
21. P.T. Tho J.R. Byrd P.G. McDonough Etiologies and subsequent reproductive performance of 100 couples with recurrent abortion Fertil Steril 32 1979 389
22. R. Gagné C. Laberge R. Tanguay Aspect cytologique et localisation intranucléaire de l’heterochromatine constitutive des chromosomes C 9 chez l’homme Chromosoma 41 1973 159
23. A. Stahl J.M. Luciani M. Devictor A.M. Capodano R. Gagné Constitutive heterochromatin and micronucleoli in the human oocyte at the diplotene stage Hum Genet (continues Humangenetik) 26 1975 315