Refined localization of autosomal recessive nonsyndromic deafness DFNB10 locus using 34 novel microsatellite markers, genomic structure, and exclusion of six known genes in the region

Genomics

Volumn 68, Issue 1, 2000, Pages 22-29

  Berry, Asher ^a   Scott, Hamish S ^b   Kudoh, Jun ^c   Talior, Ilana ^a   Korostishevsky, Michael ^a   Wattenhofer, Marie ^b   Guipponi, Michel ^b   Barras, Christine ^b   Rossier, Colette ^b   Shibuya, Kazunori ^c   Wang, Jun ^c   Kawasaki, Kazuhiko ^c   Asakawa, Shuichi ^c   Minoshima, Shinsei ^c   Shimizu, Nobuyoshi ^c   Antonarakis, Stylianos ^b   Bonné Tamir, Batsheva ^a  

^a TEL AVIV UNIVERSITY   (Israel)

^b UNIVERSITY OF GENEVA MEDICAL SCHOOL   (Switzerland)

^c KEIO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOME 21Q; CLINICAL ARTICLE; CONTROLLED STUDY; GENE LOCUS; HEARING IMPAIRMENT; HUMAN; MICROSATELLITE INSTABILITY; MOLECULAR CLONING; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

EID: 0034662762     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2000.6253     Document Type: Article

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