Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1

European Journal of Human Genetics

Volumn 11, Issue 2, 2003, Pages 185-188

  Masmoudi, Saber ^a   Tlili, Abdelaziz ^a   Majava, Marja ^b   Ghorbel, Abdel Monem ^c   Chardenoux, Sébastien ^d   Lemainque, Arnaud ^e   Zina, Zeineb Ben ^c   Moala, Jihene ^c   Männikkö, Minna ^b   Weil, Dominique ^d   Lathrop, Mark ^e   Ala Kokko, Leena ^b,f   Drira, Mohamed ^c   Petit, Christine ^d   Ayadi, Hammadi ^a  

^a UNIVERSITY OF SFAX   (Tunisia)

^b UNIVERSITY OF OULU   (Finland)

^c HABIB BOURGUIBA HOSPITAL   (Tunisia)

^d INSTITUT PASTEUR   (France)

^e CENTRE NATIONAL DE GÉNOTYPAGE   (France)

^f TULANE UNIVERSITY HEALTH SCIENCES CENTER   (United States)

Author keywords

COL11A1; DFNB32; Gene localisation; Mutation analysis; Nonsyndromic hearing impairment

Indexed keywords

COMPLEMENTARY DNA;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 1; CHROMOSOME 1P; CLINICAL ARTICLE; CONSANGUINITY; CONTROLLED STUDY; DATA BASE; DNA FLANKING REGION; DNA LIBRARY; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC ANALYSIS; GENETIC CODE; GENETIC DISORDER; GENETIC LINKAGE; GENETIC POLYMORPHISM; GENETIC SCREENING; GENETIC TRAIT; GENOTYPE; HAPLOTYPE; HEARING LOSS; HUMAN; INDIVIDUALITY; MARSHALL SYNDROME; MICROSATELLITE MARKER; PRIORITY JOURNAL; SCORING SYSTEM; STICKLER SYNDROME; TUNISIA;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; EXPRESSED SEQUENCE TAGS; FEMALE; GENES, RECESSIVE; GENETIC MARKERS; HEARING LOSS; HUMANS; MALE; PEDIGREE;

EID: 0037299314     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200934     Document Type: Article

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