A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29

Human Genetics

Volumn 112, Issue 1, 2003, Pages 24-28

  Modamio Høybjør, Silvia ^a   Moreno Pelayo, Miguel Angel ^a   Mencía, Angeles ^a   Del Castillo, Ignacio ^a   Chardenoux, Sebastian ^b   Armenta, Daniel ^c   Lathrop, Mark ^d   Petit, Christine ^b   Moreno, Felipe ^a  

^a HOSPITAL RAMÓN Y CAJAL   (Spain)

^b CNRS   (France)

^c HOSPITAL UNIVERSITARIO PUERTA DEL MAR   (Spain)

^d CENTRE NATIONAL DE GÉNOTYPAGE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CLAUDIN; CLAUDIN 16; FIBROBLAST GROWTH FACTOR; FIBROBLAST GROWTH FACTOR 12; UNCLASSIFIED DRUG; MICROSATELLITE DNA;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL DOMINANT INHERITANCE; CHILD; CHROMOSOME; CHROMOSOME 3Q28-29; CHROMOSOME ANALYSIS; CLAUDIN 16 GENE; CLINICAL ARTICLE; CONTROLLED STUDY; DEAFNESS AUTOSOMAL DOMINANT NONSYNDROMIC HEARING LOSS; DNA SEQUENCE; EXON; FAMILIAL INCIDENCE; FAMILY STUDY; FIBROBLAST GROWTH FACTOR 12 GENE; GENE; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC CODE; GENETIC LINKAGE; HAPLOTYPE; HEARING LOSS; HETERODUPLEX ANALYSIS; HUMAN; INTRON; LINKAGE ANALYSIS; MICROSATELLITE MARKER; PRIORITY JOURNAL; SCORING SYSTEM; SPAIN; CHROMOSOME 3; CHROMOSOME ABERRATION; CHROMOSOME MAP; DOMINANT GENE; FEMALE; GENETIC RECOMBINATION; GENETICS; MALE; PEDIGREE; PERCEPTION DEAFNESS;

CHROMOSOME ABERRATIONS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 3; FEMALE; GENES, DOMINANT; HAPLOTYPES; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MICROSATELLITE REPEATS; PEDIGREE; RECOMBINATION, GENETIC;

EID: 0037932395     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-002-0836-x     Document Type: Article

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