Clinical and molecular characterization of a family affected with X-linked ocular albinism(OA1)

Ophthalmic Genetics

Volumn 18, Issue 4, 1997, Pages 175-184

  Lam, Byron L ^a   Fingert, John H ^b   Shutt, Bryce C ^c   Singleton, E Mitchell ^d   Merin, Lawrence M ^c   Brown, Harry H ^c   Sheffield, Val C ^e   Stone, Edwin M ^b  

^a UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF ARKANSAS FOR MEDICAL SCIENCES   (United States)

^c UNIVERSITY OF ARKANSAS FOR MEDICAL SCIENCES   (United States)

^d NONE   (United States)

^e UNIVERSITY OF IOWA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; ELECTRORETINOGRAPHY; FAMILY STUDY; FEMALE; GENE DELETION; GENE MUTATION; GENETIC LINKAGE; HETEROZYGOTE; HUMAN; HYPOPIGMENTATION; HYPOPLASIA; IRIS DISEASE; MALE; MARKER GENE; NYSTAGMUS; OCULAR ALBINISM; OPHTHALMOSCOPY; PERIMETRY; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; RETINA FOVEA; SCHOOL CHILD; VISUAL ACUITY; X CHROMOSOME LINKAGE;

ADULT; AGED; ALBINISM, OCULAR; CHILD; CHILD, PRESCHOOL; ELECTRORETINOGRAPHY; EYE PROTEINS; FEMALE; FOVEA CENTRALIS; FUNDUS OCULI; HUMANS; IRIS DISEASES; LINKAGE (GENETICS); MALE; MEMBRANE GLYCOPROTEINS; MIDDLE AGED; NYSTAGMUS, PATHOLOGIC; PEDIGREE; POLYMERASE CHAIN REACTION; PROSPECTIVE STUDIES; RETINAL DISEASES; VISION DISORDERS; VISUAL ACUITY; X CHROMOSOME;

EID: 0031471848     PISSN: 13816810     EISSN: 17445094     Source Type: Journal    
DOI: 10.3109/13816819709041432     Document Type: Article

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