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1 didate gene for genetic testing for X-linked nonsyndromic hearing loss.
2 the DFNA20/26 locus cause autosomal dominant nonsyndromic hearing loss.
3 to be a dominant allele of DFNA3, a dominant nonsyndromic hearing loss.
4 ion gene GJB2 (Cx26) mutations cause >50% of nonsyndromic hearing loss.
5 onnexin-deficient mice that are models DFNB1 nonsyndromic hearing loss and deafness.
6                          Autosomal recessive nonsyndromic hearing loss (ARNSHL) is the most common fo
7 and DFNB11, two loci for autosomal recessive nonsyndromic hearing loss (ARNSHL), have been mapped to
8 7, a progressive form of autosomal-recessive nonsyndromic hearing loss (ARNSHL).
9 be responsible for Pendred syndrome (PS) and nonsyndromic hearing loss associated with enlarged vesti
10 tions of LRTOMT are associated with profound nonsyndromic hearing loss at the DFNB63 locus on human c
11            DFNB61 is a recessively inherited nonsyndromic hearing loss caused by mutations in SLC26A5
12 ed as causing progressive autosomal dominant nonsyndromic hearing loss (DFNA20/26), highlighting thes
13  kindred, dominant, adult-onset, progressive nonsyndromic hearing loss DFNA51 is due to a tandem inve
14          A gene causing autosomal-recessive, nonsyndromic hearing loss, DFNB39, was previously mapped
15 nction protein known as tricellulin, lead to nonsyndromic hearing loss (DFNB49).
16 d identification of the causative allele for nonsyndromic hearing loss DFNB82 in a consanguineous Pal
17                        Eight-eight recessive nonsyndromic hearing loss families from both American an
18 ated with post-lingual, autosomal-recessive, nonsyndromic hearing loss in humans (DFNB91).
19  30 (Cx30) have been linked to syndromic and nonsyndromic hearing loss in mice and humans.
20 fw genes and provide a model system to study nonsyndromic hearing loss in mice.
21  gene editing as a treatment for progressive nonsyndromic hearing loss in patients.
22  as a candidate gene for autosomal recessive nonsyndromic hearing loss locus 17 (DFNB17).
23 iant categorization for genetic screening of nonsyndromic hearing loss (NSHL) and other genetic disor
24                                              Nonsyndromic hearing loss (NSHL) is the most common type
25         The extreme genetic heterogeneity of nonsyndromic hearing loss (NSHL) makes genetic diagnosis
26 dentified in people with profound congenital nonsyndromic hearing loss (NSHL).
27                                Although this nonsyndromic-hearing-loss (NSHL) locus maps to the same
28  have also been found to cause low-frequency nonsyndromic hearing loss, progressive hearing loss, and
29 athogenic for dominant or recessive forms of nonsyndromic hearing loss, syndromic hearing loss, and,
30 ous Pakistani family, we detected linkage of nonsyndromic hearing loss to a 7.6 Mb region on chromoso
31 ional 40 consanguineous families segregating nonsyndromic hearing loss to the DFNB39 locus and refine
32 its a point mutation, V507D, associated with nonsyndromic hearing loss, unfolding events occur more f
33 consanguineous family segregating recessive, nonsyndromic hearing loss was used to make a library of
34 DFNA23, a novel locus for autosomal dominant nonsyndromic hearing loss, was identified in a Swiss Ger