Mutations in the CHX10 gene in non-syndromic microphthalmia/anophthalmia patients from Qatar

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Bibliographic Details
Published in:	Clinical genetics Vol. 72; no. 2; pp. 164 - 166
Main Authors:	Faiyaz-Ul-Haque, M, Zaidi, SHE, Al-Mureikhi, MS, Peltekova, I, Tsui, L-C, Teebi, AS
Format:	Journal Article
Language:	English
Published:	Oxford, UK Blackwell Publishing Ltd 01-08-2007 Blackwell
Subjects:	Anophthalmos - genetics Base Sequence Biological and medical sciences Consanguinity Fundamental and applied biological sciences. Psychology General aspects. Genetic counseling Genetics of eukaryotes. Biological and molecular evolution Homeodomain Proteins - genetics Humans Malformations of the eye Medical genetics Medical sciences Microphthalmos - genetics Molecular and cellular biology Molecular Sequence Data Mutation Ophthalmology Pedigree Qatar Sequence Analysis Transcription Factors - genetics Asia Qatar Human Eye disease Gene Malformation Genetics Patient Mutation Congenital disease Anophthalmos Microphthalmia
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Bibliography:	ArticleID:CGE846 istex:501B74F98FEB8C29DAC41B9672C2ED4DF2161786 ark:/67375/WNG-HKPHDMZQ-P ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 SourceType-Other Sources-1 content type line 63 ObjectType-Correspondence-1
ISSN:	0009-9163 1399-0004
DOI:	10.1111/j.1399-0004.2007.00846.x