Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences-Reference-Cited by-同舟云学术

Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences

Published:1990-03 Issue:3 Volume:35 Page:333-349
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Magenis R. E.,Toth-Fejel S.,Allen L. J.,Black M.,Brown M. G.,Budden S.,Cohen R.,Friedman J. M.,Kalousek D.,Zonana J.,Lacy D.,Lafranchi S.,Lahr M.,Macfarlane J.,Williams C. P. S.

Publisher

Wiley

Subject

Genetics (clinical)

Reference39 articles.

1. ‘Puppet’ Children A Report on Three Cases

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

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

4. Identification of human chromosomes by DNA-binding fluorescent agents

5. Prader-Willi syndrome

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