Parental origin of chromosome 5 deletions in the cri-du-chat syndrome-Reference-Cited by-同舟云学术

Parental origin of chromosome 5 deletions in the cri-du-chat syndrome

Published:1990-09 Issue:1 Volume:37 Page:83-86
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Overhauser J.,McMahon J.,Oberlender S.,Carlin M. E.,Niebuhr E.,Wasmuth J. J.,Lee-Chen J.

Publisher

Wiley

Subject

Genetics (clinical)

Reference21 articles.

1. PARENTAL ORIGIN OF CHROMOSOME 15 DELETION IN PRADER-WILLI SYNDROME

2. (1990): The improved prognosis in cri-du-chat (5p -) syndrome. In (ed) “Proc. 8th Cong Inter. Assoc. for the Scientific Study of Mental Deficiency.” Edinburgh, Scotland: Blackwell Sci. Publ. Ltd.

3. Linkage of theleuS, emtB, andchr genes on chromosome 5 in humans and expression of human genes encoding protein synthetic components in human-Chinese hamster hybrids

4. Selective linkage disruption in human-Chinese hamster cell hybrids: deletion mapping of the leuS, hexB, emtB, and chr genes on human chromosome 5.

5. A genetic linkage map of the human genome

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