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1 a region overlapping the DFNB7/B11 locus for recessive deafness.
2 esorption in the kidney, and cause autosomal recessive deafness.
3 e observed in the families with nonsyndromic recessive deafness.
4 e mutation that cosegregated with congenital recessive deafness.
5 the GJB2 gene cause one form of nonsyndromic recessive deafness.
6 15 cause Usher Syndrome (deaf-blindness) and recessive deafness.
9 afness, we screened 25 Chinese families with recessive deafness and identified in two families affect
14 bled the frequency of the commonest forms of recessive deafness (DFNB1) in this country during the pa
18 ng modifiers include DFNM1, which suppresses recessive deafness DFNB26, and a nuclear gene that modul
19 mutations in CLDN14 that cause nonsyndromic recessive deafness DFNB29 in two large consanguineous Pa
20 human pejvakin gene that cause nonsyndromic recessive deafness (DFNB59) by affecting the function of
22 deletion encompassing exon 14 of Tmc1 in the recessive deafness (dn) mouse mutant, which lacks audito
23 Ashkenazi Jewish families with nonsyndromic recessive deafness, from Ashkenazi Jewish persons seekin
26 nt for the majority of cases of nonsyndromic recessive deafness in the Ashkenazi Jewish population.
30 FNB3, a locus for nonsyndromic sensorineural recessive deafness, maps to a 3-centimorgan interval on
33 nal myosin, myosin VIIA, underlies the mouse recessive deafness mutation, shaker-1 as well as Usher s
35 inant or recessive skin disease, dominant or recessive deafness or dominant neuropathy with deafness.
36 ore than 80 percent of cases of nonsyndromic recessive deafness result from inheritance of the 30delG
37 families segregating nonsyndromic autosomal recessive deafness were analyzed to refine the DFNB12 lo
38 regions associated with human autosomal and recessive deafness, which may prove useful for the ident
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