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Prenatal diagnosis of 5p-.

作者信息

David K, Kaffe S, Strauss L, Hsu L Y, Serotkin A, Hirschhorn K

出版信息

Clin Genet. 1978 Feb;13(2):224-8. doi: 10.1111/j.1399-0004.1978.tb04253.x.

DOI:10.1111/j.1399-0004.1978.tb04253.x
PMID:627112
Abstract

With the combination of the various banding techniques (G,Q, and R), a small deletion of the short arm of a No.5 chromosome was detected prenatally in the pregnancy of a 39-year-old woman. The deletion appeared to be either intersitial in nature, involving part of p13 and p14, or the result of a translocation with deletion of p13 leads to pter. Both parents were found to have a normal chromosome constitution with normal banding patterns. Thus, this deletion was a de novo event. Repeat amniotic fluid cell chromosome analysis at the time of elective abortion, and postmortem examination of the fetus confirmed the prenatal cytogenetic diagnosis. We wish to emphasize that precise identification of a small deletion, as in this case, requires a combination of the various banding techniques.

摘要

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引用本文的文献

1
The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features.猫叫综合征:流行病学、细胞遗传学及临床特征
Hum Genet. 1978 Nov 16;44(3):227-75. doi: 10.1007/BF00394291.