New locus for autosomal dominant high myopia maps to the long arm of chromosome 17

Investigative Ophthalmology and Visual Science

Volumn 44, Issue 5, 2003, Pages 1830-1836

  Paluru, Prasuna ^a   Ronan, Sbawn M ^b   Heon, Elise ^c   Devoto, Marcella ^d,e   Wildenberg, Scott C ^b   Scavello, Genaro ^a   Holleschau, Ann ^b   Mäkitie, Outi ^f   Cole, William G ^f   King, Richard A ^g   Young, Terri L ^a,b,h  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b UNIVERSITY OF MINNESOTA   (United States)

^c UNIVERSITY HEALTH NETWORK   (Canada)

^d NEMOURS ALFRED I DUPONT HOSPITAL FOR CHILDREN   (United States)

^e UNIVERSITY OF GENOA   (Italy)

^f HOSPITAL FOR SICK CHILDREN   (Canada)

^g UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^h CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTERIOR EYE CHAMBER DISEASE; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 12Q; CHROMOSOME 17; CHROMOSOME 18P; CHROMOSOME 7Q; CHROMOSOME ARM; CLINICAL ARTICLE; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; DISEASE SEVERITY; DNA FLANKING REGION; EHLERS DANLOS SYNDROME; FAMILY; FEMALE; GENE LOCUS; GENE MAPPING; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC SCREENING; GENOME; GENOTYPE; GLAUCOMA; HAPLOTYPE; HUMAN; MALE; MARFAN SYNDROME; MICROSATELLITE MARKER; MYOPIA; PRIORITY JOURNAL; REFRACTION ERROR; SCORING SYSTEM; STICKLER SYNDROME;

CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; GENES, DOMINANT; GENOTYPE; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MICROSATELLITE REPEATS; MYOPIA; PEDIGREE; QUANTITATIVE TRAIT LOCI;

EID: 0242500304     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: 10.1167/iovs.02-0697     Document Type: Article

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