A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25

Human Genetics

Volumn 110, Issue 4, 2002, Pages 348-350

  Mustapha, Mirna ^a   Chouery, Éliane ^b   Torchard Pagnez, Delphine ^e   Nouaille, Sylvie ^a   Khrais, Awni ^c   Sayegh, Fouad N ^d   Mégarbané, André ^b   Loiselet, Jacques ^b   Lathrop, Mark ^e   Petit, Christine ^a   Weil, Dominique ^a  

^a CNRS   (France)

^b SAINT JOSEPH UNIVERSITY   (Lebanon)

^c Ibn Al Haytham Hospital   (Jordan)

^d Jabal Amman   (Jordan)

^e CENTRE NATIONAL DE GÉNOTYPAGE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ALLELE; ARAB; ARTICLE; CASE REPORT; CHROMOSOME 17Q; CHROMOSOME 17Q24-25; CIRCLING BEHAVIOR; CLINICAL FEATURE; CONSANGUINITY; DISEASE CLASSIFICATION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC SCREENING; HEARING IMPAIRMENT; HEARING LOSS; HUMAN; HUMAN GENOME; JORDAN; LINKAGE ANALYSIS; MOUSE MUTANT; PRESCHOOL CHILD; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; USHER SYNDROME; VESTIBULAR DISORDER;

ADULT; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; LINKAGE (GENETICS); MALE; PEDIGREE; RETINITIS PIGMENTOSA; SYNDROME;

MURINAE;

EID: 0036556270     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-002-0690-x     Document Type: Article

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