Refined mapping of the gene for autosomal dominant retinitis pigmentosa (RP17) on chromosome 17q22

Human Genetics

Volumn 104, Issue 1, 1999, Pages 73-76

  Den Hollander, Anneke I ^a   Van Der Velde Visser, Saskia D ^a   Pinckers, Alfred J L G ^a   Hoyng, Carel B ^a   Brunner, Han G ^a   Cremers, Frans P M ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

AMINE OXIDASE (FLAVIN CONTAINING); TRANSDUCIN;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 17Q; CLINICAL ARTICLE; FAMILY STUDY; FEMALE; GENE MAPPING; HUMAN; MALE; PEDIGREE; PRIORITY JOURNAL; RETINITIS PIGMENTOSA;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; GENES, DOMINANT; GENETIC MARKERS; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); MALE; PEDIGREE; PHENOTYPE; RECOMBINATION, GENETIC; RETINITIS PIGMENTOSA;

EID: 0033009634     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050912     Document Type: Article

References (14)

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