Autosomal dominant congenital nystagmus is not linked to 6p12, 7p11, and 15q11 in a German family

American Journal of Ophthalmology

Volumn 138, Issue 3, 2004, Pages 439-443

  Hoffmann, Steve ^a   Becker, Andreas ^a   Hoerle, Steffen ^a   Metz, Aline ^a   Oertel, Wolfgang H ^a   Sommer, Norbert ^a   Hemmer, Bernhard ^a,b  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

^b HEINRICH HEINE UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 15Q; CHROMOSOME 6P; CHROMOSOME 7P; CLINICAL ARTICLE; CONGENITAL NYSTAGMUS; FAMILY HISTORY; FEMALE; FOLLOW UP; GENE LOCUS; GENE TRANSLOCATION; GENETIC LINKAGE; GERMANY; HUMAN; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; OCULOGRAPHY; PEDIGREE ANALYSIS; PRIORITY JOURNAL;

CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 6; CHROMOSOMES, HUMAN, PAIR 7; DNA; ELECTROOCULOGRAPHY; FEMALE; GENES, DOMINANT; GENETIC MARKERS; GERMANY; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); MALE; NYSTAGMUS, CONGENITAL; PEDIGREE; POLYMERASE CHAIN REACTION; VISUAL ACUITY;

EID: 4444292644     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ajo.2004.04.065     Document Type: Article

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