Cytogenetic survey in couples with recurrent fetal wastage

Human Genetics

Volumn 65, Issue 4, 1984, Pages 336-354

  Fryns, J P ^a   Kleczkowska, A ^b   Kubien E ^b   Petit, P ^a   Van den Berghe, H ^a  

^a Centre of Human Genetics   (Belgium)

^b MEDICAL UNIVERSITY OF LUBLIN   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME; CHROMOSOME BREAKAGE; CHROMOSOME INVERSION; CHROMOSOME TRANSLOCATION; CHROMOSOME VARIANT; CLINICAL ARTICLE; ETIOLOGY; FEMALE GENITAL SYSTEM; FETUS WASTAGE; GENETIC COUNSELING; HEREDITY; HETEROZYGOTE; HISTOLOGY; HUMAN; POLYMORPHISM; PREGNANCY; ROBERTSONIAN CHROMOSOME TRANSLOCATION; SEX DIFFERENCE; SPONTANEOUS ABORTION;

ABORTION, HABITUAL; CHROMOSOME ABERRATIONS; FEMALE; FETAL DEATH; HETEROZYGOTE; HUMANS; INVERSION, CHROMOSOME; KARYOTYPING; MALE; PEDIGREE; POLYMORPHISM, GENETIC; PREGNANCY; SEX FACTORS; TRANSLOCATION, GENETIC;

ROBERTSONIA;

EID: 0021336773     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/BF00291558     Document Type: Article

References (62)

1. Les recherches cytogénétiques chez les sujets ayant des échecs de la reproduction
2. Systematic analysis of 95 reciprocal translocations of autosomes
3. Minor chromosomal variants and major chromosomal anomalies in couples with recurrent abortion
4. Cytogenetic survey of couples with habitual abortion and other reproductive wastage
5. Chromosome structural rearrangements and reproductive failure
6. Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families
7. Diagnostic prénatal des anomalies de la structure chromosomique
8. Chromosomenanomalien bei Ehepaaren mit wiederholten Aborten
9. The origin of chromosomal aberrations in man and their potential for survival and reproduction in the adult human population
10. Pericentric inversions of human chromosomes 9 and 10
11. Balanced translocation karyotypes in patients with repetitive abortion
12. The importance of cytogenetic investigation of the couples with multiple spontaneous abortions and malformed offsprings
13. Etude de la descendance des individus porteurs d'une translocation t(Dq;Dq)
14. Within pair differences of human chromosome 9C-bands associated with reproductive loss
15. Cytogenetics of human male infertility
16. Male infertility and 13/14 translocation
17. Malformative syndrome associated with a ring 10 chromosome and a translocated 10q/19 chromosome
18. Fertility in patients with X chromosome deletions
19. Small accessory chromosomes (SAC) and their genotype-phenotype correlation
20. Paracentric inversion in man: Personal experience and review of the literature
21. Trisomy 12q due to familial t(12p-6q+) translocation
22. New chromosomal syndrome
23. Phenotypic variation in two patients with a ring chromosome 22
24. Cytogenetic studies of the leukocytes of couples with habitual abortions
25. Heterochromatic polymorphism in spontaneous abortions
26. Cytogenetics of recurrent abortions
27. Marker chromosomes in parents of spontaneous abortuses
28. Chromosome abnormalities in 150 couples with multiple spontaneous abortions
29. An analysis of the breakpoints of structural rearrangements in man
30. Cytogenetics of aborters and abortuses
31. Incidence of chromosomal rearrangements in couples with reproductive loss
32. Geneticzeskije isledovanja pri privycznom nievynaszivanii bieremiennosti
33. Badania cytogenetyczne u malźeństw z niepowodzeniami poloźniczymi
34. Meiosis in a man with a D/D translocation and clinical sterility
35. Complex chromosomal rearrangements (CCR) and their genetic consequences
36. Balanced translocations among couples with two or more spontaneous abortions: are males and females equally likely to be carriers
37. Cytogenetics of recurrent abortions
38. Semen analysis in subfertile balanced-translocation carriers
39. An evaluation of cytogenetic analysis as a primary tool in the assessment of recurrent pregnancy wastage
40. Chromosome translocations in couples with multiple spontaneous abortions
41. 13/14 translocation in a man with reproductive failure
42. Incidenza della variante 9qh+ in soggetti professionalmente radioesposti ed in casi di patologia riproduttiva
43. Chromosome analysis in cases with repeated spontaneous abortions
44. Frequency of 9qh+ and risk of chromosome aberrations in the progeny of individuals with 9qh+
45. Increased frequencies of chromosomal abnormalities in families with a history of fetal wastage
46. Cytogenetic investigations in 418 couples with recurrent fetal wastage
47. Fausses-couches précoces itératives et caryotype. Etude cytogénétique de 80 couples consécutifs
48. The association of D-group chromosomal translocations and defective spermatogenesis
49. Chromosomes in familial primary sterility and in couples with recurrent abortions and stillbirth
50. Chromosomal analysis of couples with repeated spontaneous abortions
51. Parental chromosomal rearrangements associated with repetitive spontaneous abortions
52. Cytogenetics of habitual abortion and other reproductive wastage
53. Nonrandom distribution of exchange points in patients with reciprocal translocations
54. Cytogenetic findings in 122 couples with recurrent abortions
55. Segregation of a 22 ring chromosome in three generations
56. Chromosomal polymorphic variants in couples with recurrent spontaneous abortions
57. Etiologies and subsequent reproductive performance of 100 couples with recurrent abortion
58. Pericentric inversion of chromosome 9 in couples with repeated spontaneous abortion
59. Parental chromosome translocations and fetal loss
60. Chromosome studies in couples with repeated spontaneous abortions
61. Cytogenetic investigation in 413 couples with spontaneous abortions
62. Cytogenetic studies in 100 couples with recurrent spontaneous abortions