DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1

European Journal of Human Genetics

Volumn 11, Issue 10, 2003, Pages 816-818

  Delmaghani, Sedigheh ^a   Aghaie, Asadollah ^a   Compain Nouaille, Sylvie ^a   Ataie, Afsaneh ^b   Lemainque, Arnaud ^c   Zeinali, Sirous ^d   Lathrop, Mark ^c   Weill, Dominique ^a   Petit, Christine ^a  

^a INSTITUT PASTEUR   (France)

^b Specialised Education Center   (Iran)

^c CENTRE NATIONAL DE GÉNOTYPAGE   (France)

^d PASTEUR INSTITUTE OF IRAN   (Iran)

Author keywords

Chromosome 22; Gene localization; Human deafness

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BEHAVIOR DISORDER; CASE REPORT; CHROMOSOME 22Q; CHROMOSOME 5; CHROMOSOME MAP; CONSANGUINITY; GENE LOCUS; GENETIC DISTANCE; GENOTYPE; HAIR CELL; HEARING IMPAIRMENT; HUMAN; INNER EAR DISEASE; IRAN; LINKAGE ANALYSIS; MOUSE MUTANT; PERCEPTION DEAFNESS; PRIORITY JOURNAL; PURE TONE AUDIOMETRY; SCHOOL CHILD;

ADOLESCENT; ADULT; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; GENES, RECESSIVE; GENETIC MARKERS; GENOTYPE; HEARING LOSS, SENSORINEURAL; HUMANS; LOD SCORE; MALE; MUTATION; PEDIGREE;

IRANIA; MURINAE;

EID: 0242351070     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201045     Document Type: Article

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