Prenatal diagnosis of translocation and a single pericentric inversion 9: The value of fetal ultrasound

Journal of Obstetrics and Gynaecology

Volumn 21, Issue 5, 2001, Pages 474-477

  Salihu, H M ^a   Boos, R ^a   Tchuinguem, G ^a   Schmidt, W ^a  

^a NATIONAL SCHOOL OF PUBLIC HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHROMOSOME INVERSION 9; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; CROSSING OVER; FEMALE; FETUS ECHOGRAPHY; GENE DELETION; GENE DUPLICATION; GENE REARRANGEMENT; GENETIC COUNSELING; HETEROCHROMATIN; HIGH RISK PREGNANCY; HUMAN; KARYOTYPE; PERICENTRIC CHROMOSOME INVERSION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

EID: 0034813822     PISSN: 01443615     EISSN: None     Source Type: Journal    
DOI: 10.1080/01443610120072018     Document Type: Article

References (10)

1. Polymorphism of human constitutive heterochromatin
2. Aneusomie de recombinaison: Three further examples
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4. Chromosomal polymorphism of 1,9,16, and Y in 4 major ethnic groups: A large prenatal study
5. Pericentric inversions. Problems and significance for clinical genetics
6. Chromosome translocations in couples with multiple spontaneous abortions
7. Chromosome studies of 500 couples with two or more abortions
8. A cross-over reducer in Drosophila melanogaster due to inversion of a section of the third chromosome
9. The outcome of pregnancy and prenatal chromosomal diagnosis of fetuses in couples including a translocation carrier