Clinical utility gene card for: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches-Reference-Cited by-同舟云学术

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Clinical utility gene card for: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches

Published:2017-01-18 Issue:4 Volume:25 Page:512-512
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Richardson Rose,Sowden Jane,Gerth-Kahlert Christina,Moore Anthony T,Moosajee Mariya

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg2016201.pdf

Reference58 articles.

1. Verma AS, Fitzpatrick DR : Anophthalmia and microphthalmia. Orphanet J Rare Dis 2007; 2: 47.

2. Weiss AH, Kousseff BG, Ross EA, Longbottom J : Complex microphthalmos. Arch Ophthalmol 1989; 107: 1619–1624.

3. Nishina S, Kurosaka D, Nishida Y, Kondo H, Kobayashi Y, Azuma N : Survey of microphthalmia in Japan. Jpn J Ophthalmol 2012; 56: 198–202.

4. Forrester MB, Merz RD : Descriptive epidemiology of anophthalmia and microphthalmia, Hawaii, 1986-2001. Birth Defects Res A Clin Mol Teratol 2006; 76: 187–192.

5. Morle L, Bozon M, Zech JC et al: A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15. Am J Hum Genet 2000; 67: 1592–1597.

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