DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22-q21.12

European Journal of Human Genetics

Volumn 11, Issue 10, 2003, Pages 812-815

  Wajid, Muhammad ^a   Abbasi, Amir Ali ^a   Ansar, Muhammad ^a   Pham, Thanh L ^b   Yan, Kai ^b   Haque, Sayedul ^a   Ahmad, Wasim ^a   Leal, Suzanne M ^b  

^a QUAID I AZAM UNIVERSITY   (Pakistan)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

7q11.22 q21.12; Autosomal recessive nonsyndromic hearing impairment; DFNB39; Linkage mapping; Pakistan

Indexed keywords

DNA;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 7Q; CHROMOSOME MAP; CONSANGUINITY; CONTROLLED STUDY; GENE LOCUS; GENOTYPE; HOMOZYGOSITY; HUMAN; LINKAGE ANALYSIS; MICROSATELLITE MARKER; NONVERBAL COMMUNICATION; PAKISTAN; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SCORING SYSTEM;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 7; FEMALE; GENES, RECESSIVE; GENETIC MARKERS; HAPLOTYPES; HEARING LOSS, SENSORINEURAL; HOMOZYGOTE; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; PAKISTAN; PEDIGREE;

EID: 0242319675     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201041     Document Type: Article

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