Results 71 to 80 of about 139 (86)
Some of the next articles are maybe not open access.
DFNB3 Families and <i>Shaker</i>-2 Mice: Mutations in an Unconventional Myosin, <i>MYO 15</i>
2000T.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, 2012Dana Šafka Brožková +2 more
exaly
DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22–q21.12
European Journal of Human Genetics, 2003Muahmmad Ansar +2 more
exaly
DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15.
Advances in oto-rhino-laryngology, 2000T B, Friedman +5 more
openaire +1 more source
Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39
American Journal of Human Genetics, 2009Muahmmad Ansar +2 more
exaly
Re-assigning the DFNB33 locus to chromosome 10p11.23–q21.1
European Journal of Human Genetics, 2008Myrna Medlej-Hashim +2 more
exaly

