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American Journal of Ophthalmology

Volumn 125, Issue 1, 1998, Pages 64-70

Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12

(5) Kerrison, John B b Koenekoop, Robert K a Arnould, Véronique J c,d,e Zee, David f Maumenee, Irene H a,f,g

a JOHNS HOPKINS UNIVERSITY (United States)

b Research to Prevent Blindness Inc (United States)

c Belg Amer Educational Foundation (Belgium)

d Belgian Rotary Foundation (Belgium)

e Vocational Foundation of Belgium (Belgium)

f NATIONAL INSTITUTES OF HEALTH (United States)

g JOHNS HOPKINS UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CHROMOSOME 16P; CLINICAL FEATURE; CONGENITAL NYSTAGMUS; ELECTRORETINOGRAPHY; EVOKED VISUAL RESPONSE; EYE MOVEMENT; FEMALE; GENE EXPRESSION; GENETIC LINKAGE; HUMAN; MAJOR CLINICAL STUDY; MALE; PEDIGREE; PRIORITY JOURNAL; SCANNING LASER OPHTHALMOSCOPY; STRABISMUS; VISUAL ACUITY;

EID: 0031964691 PISSN: 00029394 EISSN: None Source Type: Journal
DOI: 10.1016/S0002-9394(99)80236-0 Document Type: Article

Times cited : (42)

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