Affordable Access

[HOXD13 polyalanine tract expansion in synpolydactyly: mutation detection and prenatal diagnosis in a large Chinese family].

Authors
  • Zhao, Xiu-li
  • Meng, Jin-ping
  • Sun, Miao
  • Ao, Yang
  • Wu, Ai-hua
  • Lo, H Y Wilson
  • Zhang, Xue
Type
Published Article
Journal
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Publication Date
Feb 01, 2005
Volume
22
Issue
1
Pages
5–9
Identifiers
PMID: 15696469
Source
Medline
License
Unknown

Abstract

HOXD13 polyalanine expansion was detected in a large Chinese family with SPD and prenatal diagnosis of two affected fetuses was achieved. This is the first report on prenatal diagnosis of SPD by detecting the HOXD13 polyalanine expansion in the Han population of the Chinese mainland.

Report this publication

Statistics

Seen <100 times