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Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations.
Forshew, Tim; Johnson, Colin A; Khaliq, Shagufta; Pasha, Shanaz; Willis, Catherine; Abbasi, Rashida; Tee, Louise; Smith, Ursula; Trembath, Richard C; Mehdi, Syed Qasim; Moore, Anthony T; Maher, Eamonn R.
Affiliation
  • Forshew T; Section of Medical and Molecular Genetics, Institute of Biomedical Research, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
Hum Genet ; 117(5): 452-9, 2005 Sep.
Article in En | MEDLINE | ID: mdl-15959809
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Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / Cataract / Chromosomes, Human, Pair 9 / Germ-Line Mutation / DNA-Binding Proteins / Genetic Linkage Type of study: Prognostic_studies Limits: Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Hum Genet Year: 2005 Document type: Article Affiliation country: United kingdom Country of publication: Germany
Search on Google
Add to My VHL
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / Cataract / Chromosomes, Human, Pair 9 / Germ-Line Mutation / DNA-Binding Proteins / Genetic Linkage Type of study: Prognostic_studies Limits: Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Hum Genet Year: 2005 Document type: Article Affiliation country: United kingdom Country of publication: Germany