GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome-Reference-Cited by-同舟云学术

GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome

Published:2001 Issue:2 Volume:102 Page:161-168
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Li Madeline,Shuman Cheryl,Fei Yan Ling,Cutiongco Eva,Bender H.A.,Stevens C.,Wilkins-Haug L.,Day-Salvatore D.,Yong S.L.,Geraghty M.T.,Squire Jeremy,Weksberg Rosanna

Publisher

Wiley

Subject

Genetics(clinical)

Reference44 articles.

1. A new X-linked dysplasia gigantism syndrome: Identical with the Simpson dysplasia syndrome?

2. Mapping of a New SGBS Locus to Chromosome Xp22 in a Family with a Severe Form of Simpson-Golabi-Behmel Syndrome

3. Extending the overlap of three congenital overgrowth syndromes

4. Integral membrane heparan sulfate proteoglycans

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