Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion-Reference-Cited by-同舟云学术

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Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

Published:1989-02 Issue:2 Volume:32 Page:285-290
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Knoll J. H. M.,Nicholls R. D.,Magenis R. E.,Graham J. M.,Lalande M.,Latt S. A.,Opitz John M.,Reynolds James F.

Publisher

Wiley

Subject

Genetics (clinical)

Reference20 articles.

1. ‘Puppet’ Children A Report on Three Cases

2. The "happy puppet" syndrome.

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

4. Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome

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