A variety of genetic mechanisms are associated with the Prader-Willi syndrome-Reference-Cited by-同舟云学术

A variety of genetic mechanisms are associated with the Prader-Willi syndrome

Published:1994-09-15 Issue:3 Volume:54 Page:219-226
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Woodage Trevor,Deng Ze-Min,Prasad Madhuri,Smart Robert,Lindeman Robert,Christian Susan L.,Ledbetter David H.,Robson Lisa,Smith Arabella,Trent Ronald J.

Publisher

Wiley

Subject

Genetics (clinical)

Reference39 articles.

1. Systematic cloning of human minisatellites from ordered array charomid libraries

2. The CEPH consortium linkage map of human chromosome 15q

3. Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial angelman syndrome

4. Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within thePWCR

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