Chromosome studies in 2136 couples with spontaneous abortions

Human Genetics

Volumn 74, Issue 4, 1986, Pages 399-401

  Bourrouillou, G ^a   Colombies, P ^a   Dastugue, N ^a  

^a CHU PURPAN   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME ABERRATION; DIAGNOSIS; ETIOLOGY; FEMALE GENITAL SYSTEM; HEREDITY; HISTOLOGY; HUMAN; KARYOTYPE; MAJOR CLINICAL STUDY; PREGNANCY; PRIORITY JOURNAL; SPONTANEOUS ABORTION;

ABORTION, SPONTANEOUS; CHROMOSOME ABERRATIONS; FEMALE; HUMAN; INFANT, NEWBORN; INVERSION (GENETICS); MALE; PREGNANCY; SEX CHROMOSOME ABERRATIONS; TRANSLOCATION (GENETICS);

EID: 0022903357     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/BF00280493     Document Type: Article

References (10)

1. Trisomie 21 et l'inversion péricentrique du chromosome 9 dans le caryotype parental
2. Cytogenetic survey in couples with recurrent fetal wastage
3. Femme 45,X/46,X,del(X)(q25) accouchée d'une fille normale 46,XX
4. The frequency of chromosome abnormalities detected in consecutive newborn studies. Differences between studies. Results by sex and severity of phenotypic involvements
5. Chromosome abnormalities in 150 couples with multiple spontaneous abortions
6. Chromosomes et infertilité, étude de 7672 cas
7. Cytogenetic investigations in 418 couples with recurrent fetal wastage
8. Chromosomal findings in 164 couples with repeated spontaneous abortions: with special consideration to prior reproductive history
9. Rôle des translocations parentales en cas de fausses couches à répètition
10. Cytogenetic investigation in 413 couples with spontaneous abortions