A new locus for autosomal dominant familial exudative vitreoretinopathy maps to chromosome 11p12-13

American Journal of Human Genetics

Volumn 68, Issue 3, 2001, Pages 778-781

  Downey, L M ^a   Keen, T J ^a   Roberts, E ^a   Mansfield, D C ^b   Bamashmus, M ^b   Inglehearn, C F ^a  

^a ST JAMES S UNIVERSITY HOSPITAL   (United Kingdom)

^b INVERCLYDE ROYAL HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR GATA 3;

ANGIOGENESIS; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 11P; CHROMOSOME MAP; CLINICAL ARTICLE; FAMILIAL DISEASE; FEMALE; GENE LOCUS; GENETIC COUNSELING; GENETIC PREDISPOSITION; HUMAN; MALE; NEUROEPITHELIUM; PEDIGREE; PRIORITY JOURNAL; RETINA BLOOD VESSEL; RETROLENTAL FIBROPLASIA; STATISTICAL ANALYSIS; VITREORETINOPATHY;

EID: 0035092388     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/318790     Document Type: Article

References (17)

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2. Familial exudative vitreoretinopathy
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7. X-linked exudative vitreoretinopathy: Clinical features and genetic linkage analysis
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15. Racial variation in retinopathy of prematurity
16. Linkage and candidate gene analysis of X-linked familial exudative vitreoretinopathy
17. Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity