Refined mapping of the usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and identification of the putative mouse homologous region

Genomics

Volumn 38, Issue 3, 1996, Pages 255-263

  Joensuu, Tarja ^d   Blanco, Gonzalo ^a   Pakarinen, Leenamaija ^d   Sistonen, Pertti ^b   Kääriäinen, Helena ^c   Brown, Steve ^a   De La Chapelle, Albert ^d   Sankila, Eeva Marja ^d  

^a MRC Mouse Genome Centre   (United Kingdom)

^b FINNISH RED CROSS BLOOD SERVICE   (Finland)

^c Vaestoliitto   (Finland)

^d NONE

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; CONTIG; DNA FRAGMENT; PROFILIN;

ANIMAL CELL; ARTICLE; CHROMOSOME 3Q; CLINICAL ARTICLE; DNA POLYMORPHISM; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENE SEGREGATION; GENETIC LINKAGE; GENETIC RECOMBINATION; HUMAN; HUMAN CELL; MOUSE; NONHUMAN; PEDIGREE; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; USHER SYNDROME; YEAST ARTIFICIAL CHROMOSOME;

EID: 0030589629     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0626     Document Type: Article

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