ライフサイエンスコーパス: nonsyndromic hearing loss

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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 onnexin-deficient mice that are models DFNB1 nonsyndromic hearing loss and deafness.

5 Autosomal recessive nonsyndromic hearing loss (ARNSHL) is the most common fo

6 and DFNB11, two loci for autosomal recessive nonsyndromic hearing loss (ARNSHL), have been mapped to

7 7, a progressive form of autosomal-recessive nonsyndromic hearing loss (ARNSHL).

8 be responsible for Pendred syndrome (PS) and nonsyndromic hearing loss associated with enlarged vesti

9 tions of LRTOMT are associated with profound nonsyndromic hearing loss at the DFNB63 locus on human c

10 ed as causing progressive autosomal dominant nonsyndromic hearing loss (DFNA20/26), highlighting thes

11 kindred, dominant, adult-onset, progressive nonsyndromic hearing loss DFNA51 is due to a tandem inve

12 A gene causing autosomal-recessive, nonsyndromic hearing loss, DFNB39, was previously mapped

13 nction protein known as tricellulin, lead to nonsyndromic hearing loss (DFNB49).

14 d identification of the causative allele for nonsyndromic hearing loss DFNB82 in a consanguineous Pal

15 Eight-eight recessive nonsyndromic hearing loss families from both American an

16 ated with post-lingual, autosomal-recessive, nonsyndromic hearing loss in humans (DFNB91).

17 30 (Cx30) have been linked to syndromic and nonsyndromic hearing loss in mice and humans.

18 fw genes and provide a model system to study nonsyndromic hearing loss in mice.

19 as a candidate gene for autosomal recessive nonsyndromic hearing loss locus 17 (DFNB17).

20 iant categorization for genetic screening of nonsyndromic hearing loss (NSHL) and other genetic disor

21 Nonsyndromic hearing loss (NSHL) is the most common type

22 The extreme genetic heterogeneity of nonsyndromic hearing loss (NSHL) makes genetic diagnosis

23 dentified in people with profound congenital nonsyndromic hearing loss (NSHL).

24 Although this nonsyndromic-hearing-loss (NSHL) locus maps to the same

25 have also been found to cause low-frequency nonsyndromic hearing loss, progressive hearing loss, and

26 athogenic for dominant or recessive forms of nonsyndromic hearing loss, syndromic hearing loss, and,

27 ous Pakistani family, we detected linkage of nonsyndromic hearing loss to a 7.6 Mb region on chromoso

28 ional 40 consanguineous families segregating nonsyndromic hearing loss to the DFNB39 locus and refine

29 consanguineous family segregating recessive, nonsyndromic hearing loss was used to make a library of

30 DFNA23, a novel locus for autosomal dominant nonsyndromic hearing loss, was identified in a Swiss Ger

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