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A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11–q13) and refined localization of the SNRPN gene

✍ Scribed by Apiwat Mutirangura; Arumugam Jayakumar; James S. Sutcliffe; Mitsuyoshi Nakao; Mary Jane Mckinney; Karin Buiting; Bernhard Horsthemke; Arthur L. Beaudet; A. Craig Chinault; David H. Ledbetter

Book ID: 117592493
Publisher: Elsevier Science
Year: 1993
Tongue: English
Weight: 1003 KB
Volume: 18
Category: Article
ISSN: 0888-7543
DOI: 10.1016/s0888-7543(11)80011-x

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Deletions of 15q11.2-q12 are associated with either the Prader-Willi (PWS) or Angelman (AS) syndromes. It has been suggested that excessive recombination in this region might explain the high frequency of such deletions, and the frequent involvement of chromosome 15 in translocations and nondisjunct