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Prenatal diagnosis of oculocutaneous albinism type II and novel mutations in two Chinese families.

Authors
  • Hongyi, Li
  • Haiyun, Wei
  • Hui, Zheng
  • Qing, Wenren
  • Honglei, Duan
  • Shu, Meng
  • Weiying, Jiang
Type
Published Article
Journal
Prenatal diagnosis
Publication Date
Jun 01, 2007
Volume
27
Issue
6
Pages
502–506
Identifiers
PMID: 17385796
Source
Medline
License
Unknown

Abstract

This is the first report of prenatal diagnosis performed in families with oculocutaneous albinism type II (OCA2). Also, this report reveals three novel mutations of the P gene.

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