Results 71 to 80 of about 139 (86)
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DFNB3 Families and <i>Shaker</i>-2 Mice: Mutations in an Unconventional Myosin, <i>MYO 15</i>

2000
T.B. Friedman   +5 more
openaire   +1 more source

DFNB35 due to a novel mutation in the gene in a Czech consanguineous family

International Journal of Pediatric Otorhinolaryngology, 2012
Dana Šafka Brožková   +2 more
exaly  

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

European Journal of Human Genetics, 2003
Masmoudi Saber   +2 more
exaly  

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

European Journal of Human Genetics, 2003
Muahmmad Ansar   +2 more
exaly  

DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15.

Advances in oto-rhino-laryngology, 2000
T B, Friedman   +5 more
openaire   +1 more source

Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39

American Journal of Human Genetics, 2009
Muahmmad Ansar   +2 more
exaly  

Mutations of ESRRB Encoding Estrogen-Related Receptor Beta Cause Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB35

American Journal of Human Genetics, 2008
Muahmmad Ansar   +2 more
exaly  

MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation†

American Journal of Medical Genetics, Part A, 2007
Hans Christian Hennies   +2 more
exaly  

Re-assigning the DFNB33 locus to chromosome 10p11.23–q21.1

European Journal of Human Genetics, 2008
Myrna Medlej-Hashim   +2 more
exaly  

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