Nonsyndromic congenital retinal nonattachment gene maps to human chromosome band 10q21

American Journal of Medical Genetics

Volumn 90, Issue 2, 2000, Pages 165-168

  Ghiasvand, N M ^a,b   Kanis, A B ^c   Helms, C ^a   Sheffield, V C ^c,d   Stone, E M ^c   Donis Keller, H ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b SHAHID BEHESHTI UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^c UNIVERSITY OF IOWA   (United States)

^d UNIVERSITY OF IOWA   (United States)

Author keywords

Autosomal recessive blindness; Congenital blindness; DNA pooling strategy; Founder effect; Homozygosity mapping; Iran; Linkage disequilibrium; Nonsyndromic congenital retinal nonattachment; Retinal detachment

Indexed keywords

ANTERIOR EYE CHAMBER DEPTH; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 10Q; CHROMOSOME BAND; CLINICAL ARTICLE; CONGENITAL BLINDNESS; CONTROLLED STUDY; FEMALE; GENE LOCATION; GENE MAPPING; GENETIC LINKAGE; GENETIC MARKER; HOMOZYGOSITY; HUMAN; MALE; MICROPHTHALMIA; NYSTAGMUS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RETINA MALFORMATION;

CHROMOSOME BANDING; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 10; DNA; FEMALE; GENOME; GENOTYPE; HUMANS; MALE; PEDIGREE; RETINAL DETACHMENT;

EID: 0034677221     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(20000117)90:2<165::AID-AJMG15>3.0.CO;2-O     Document Type: Article

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