GPC3 mutations in seven patients with Simpson–Golabi–Behmel syndrome-Reference-Cited by-同舟云学术

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GPC3 mutations in seven patients with Simpson–Golabi–Behmel syndrome

Published:2007 Issue:15 Volume:143A Page:1703-1707
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Sakazume Satoru,Okamoto Nobuhiko,Yamamoto Toshiyuki,Kurosawa Kenji,Numabe Hironao,Ohashi Yuko,Kako Yuko,Nagai Toshiro,Ohashi Hirohumi

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference16 articles.

1. Analysis of Exon/Intron Structure and 400 kb of Genomic Sequence Surrounding the 5′-Promoter and 3′-Terminal Ends of the Human Glypican 3 (GPC3) Gene

2. Simpson-Golabi-Behmel syndrome: Genotype/phenotype analysis of 18 affected males from 7 unrelated families

3. Risk of tumorigenesis in overgrowth syndromes: A comprehensive review

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

5. Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.

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