✦ LIBER ✦

Uniparental disomy as the basis for an association of rare disorders

✍ Scribed by Nicholls, Robert D.

Publisher: John Wiley and Sons
Year: 1991
Tongue: English
Weight: 202 KB
Volume: 41
Category: Article
ISSN: 0148-7299
DOI: 10.1002/ajmg.1320410233

No coin nor oath required. For personal study only.

✦ Synopsis

NOTE ADDED IN PROOF

The patient with PWS and urticaria pigmentosa has recently been shown to display isodisomy for chromosome 15qllq13 and 15 qter [Nicholls et al., unpublished data]. Also, 2 additional genes potentially involved in cancer have been mapped to distal 15q (see Popescu NC,

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