A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3

American Journal of Medical Genetics

Volumn 133 A, Issue 1, 2005, Pages 18-22

  Aslam, Muhammad ^a   Wajid, Muhammad ^a   Chahrour, Maria H ^b   Ansar, Muhammad ^a   Haque, Sayedul ^a   Pham, Thanh L ^b   Santos, Regie P ^b   Yan, Kai ^b   Ahmad, Wasim ^a   Leal, Suzanne M ^b  

^a QUAID I AZAM UNIVERSITY   (Pakistan)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

3q13.31 q22.3; DFNB42; Nonsyndromic hearing impairment; Pakistan

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 3Q; CHROMOSOME MAP; CONSANGUINITY; FEMALE; GENE LOCUS; GENETIC LINKAGE; GENETIC MARKER; HEARING IMPAIRMENT; HOMOZYGOSITY; HUMAN; MALE; PRIORITY JOURNAL; SCHOOL CHILD;

AUDIOMETRY; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 3; FEMALE; GENES, RECESSIVE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HEARING LOSS; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MICROSATELLITE REPEATS; PEDIGREE;

EID: 19944430504     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30508     Document Type: Article

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