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Volumn 18, Issue 5, 1998, Pages 448-452

North Carolina macular dystrophy (MCDR1) in Texas

Author keywords

Autosomal dominant; Genetics; Haplotype analysis; Linkage analysis; Macular degeneration; Macular dystrophy; Multipoint analysis; North Carolina

Indexed keywords

ARTICLE; FAMILY STUDY; GENE MAPPING; GENE MUTATION; GENETIC LINKAGE; HAPLOTYPE; HUMAN; PEDIGREE; PHENOTYPE; RETINA MACULA DEGENERATION; UNITED STATES;

EID: 0032472006     PISSN: 0275004X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00006982-199805000-00012     Document Type: Article
Times cited : (22)

References (18)
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  • 9
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    • North Carolina macular dystrophy (NCMD) and central areolar pigment epithelial dystrophy (CAPED), one family, one disease
    • Small KW, Hermsen V, Gurney N, Fetkenhour C, Folk J. North Carolina macular dystrophy (NCMD) and central areolar pigment epithelial dystrophy (CAPED), one family, one disease. Arch Ophthalmol 1991;110:515-518.
    • (1991) Arch Ophthalmol , vol.110 , pp. 515-518
    • Small, K.W.1    Hermsen, V.2    Gurney, N.3    Fetkenhour, C.4    Folk, J.5
  • 10
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    • North Carolina macular dystrophy maps to the MCDR1 locus (MCDR1) phenotype in Central America
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.