Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers

Clinical Genetics

Volumn 66, Issue 4, 2004, Pages 358-364

  Masmoudi, S ^a   Charfedine, I ^b   Rebeh, I B ^a   Rebai, A ^c   Tlili, A ^a   Ghorbel, A M ^b   Belguith, H ^a   Petit, C ^d   Drira, M ^b   Ayadi, Hammadi ^a  

^a UNIVERSITY OF SFAX   (Tunisia)

^b HABIB BOURGUIBA HOSPITAL   (Tunisia)

^c CENTRE DE BIOTECHNOLOGIE DE SFAX   (Tunisia)

^d INSTITUT PASTEUR   (France)

Author keywords

Candidate gene; DFNB13; Linkage analyses; Microsatellite; Polymorphism

Indexed keywords

GENE PRODUCT; PROTEIN DFNB 13; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; AUDITORY SYSTEM EXAMINATION; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 7Q; CLINICAL ARTICLE; CONSANGUINITY; CONTROLLED STUDY; DINUCLEOTIDE REPEAT; DISEASE SEVERITY; EVOKED AUDITORY RESPONSE; FAMILY STUDY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENE SEQUENCE; GENETIC POLYMORPHISM; GENETIC SCREENING; HAPLOTYPE; HEARING IMPAIRMENT; HUMAN; LINKAGE ANALYSIS; MICROSATELLITE MARKER; NUCLEOTIDE SEQUENCE; PATHOGENESIS; POLYMERASE CHAIN REACTION; POPULATION RESEARCH; PREDICTION; PRIORITY JOURNAL; PURE TONE AUDIOMETRY; TUNISIA;

CASE-CONTROL STUDIES; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 7; DEAFNESS; DNA; FEMALE; GENES; GENES, RECESSIVE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; MALE; MICROSATELLITE REPEATS; PEDIGREE; TUNISIA;

EID: 4844229668     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2004.00311.x     Document Type: Article

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