A 68-year-old white female with Prader-Willi syndrome

被引：3

作者：

Butler, MG ^{[1
]}

机构：

[1] Childrens Mercy Hosp, Sect Med Genet & Mol Med, Kansas City, MO 64108 USA

来源：

CLINICAL DYSMORPHOLOGY | 2000年 / 9卷 / 01期

关键词：

Prader-Willi syndrome; cataracts; 15q11-q13; deletion; natural history;

D O I：

10.1097/00019605-200009010-00015

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

A 68-year-old white female with Prader-Willi syndrome is described. The clinical features are described and the progression of her condition is discussed and illustrated. Clin Dysmorphol 9:65-67 (C) 2000 Lippincott Williams & Wilkins.

引用

页码：65 / 67

页数：3

共 6 条

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[5] GENETIC IMPRINTING SUGGESTED BY MATERNAL HETERODISOMY IN NONDELETION PRADER-WILLI SYNDROME
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[6] Thompson Travis, 1996, Peabody J Educ, V71, P187

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