Retinitis pigmentosa locus on 17q (RP17): Fine localization to 17q22 and exclusion of the PDEG and TIMP2 genes

Human Genetics

Volumn 101, Issue 1, 1997, Pages 13-17

  Bardien, Soraya ^a   Ramesar, Rajkumar ^a   Bhattacharya, Shomi ^b   Greenberg, Jacquie ^a  

^a UNIVERSITY OF CAPE TOWN   (South Africa)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; DNA MARKER; MICROSATELLITE DNA; PHOSPHODIESTERASE; PROTEIN KINASE C; TISSUE INHIBITOR OF METALLOPROTEINASE;

ARTICLE; CHROMOSOME 17Q; DNA RECOMBINATION; FAMILY STUDY; FEMALE; GENE MAPPING; GENETIC LINKAGE; HAPLOTYPE; HUMAN; MALE; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; RETINITIS PIGMENTOSA; SINGLE STRAND CONFORMATION POLYMORPHISM;

3',5'-CYCLIC-GMP PHOSPHODIESTERASE; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; DNA PRIMERS; FEMALE; GENES, DOMINANT; HAPLOTYPES; HUMANS; ISOENZYMES; LINKAGE (GENETICS); MALE; MICROSATELLITE REPEATS; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROTEIN KINASE C; PROTEIN KINASE C-ALPHA; RETINITIS PIGMENTOSA; TISSUE INHIBITOR OF METALLOPROTEINASES;

EID: 0031456441     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050577     Document Type: Article

References (15)

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