<p>Audiogram: Right (red) and left (blue) ear hearing thresholds. Pedigree: Filled symbols represent hearing-impaired individuals, and clear symbols denote those with normal hearing. Black arrow indicates the proband. Possible arrangement of <i>CDH23</i> variants in SB116 family based on haplotype and segregation study.</p
<p>A. Patients with hearing loss caused by a c.235delC mutation (excluding patients with a p.V37I mu...
All in-text references underlined in blue are linked to publications on ResearchGate, letting you ac...
Nonsyndromic hearing loss has been shown to have high genetic heterogeneity. In this report, we aime...
<p>Pedigrees, mutations, and audiograms of the patients with compound heterozygous <i>CDH23</i> muta...
<p>Pedigrees, mutations, and audiograms of the patients with homozygous <i>CDH23</i> mutations.</p
Screening for gene mutations in CDH23, which has many exons, has lagged even though it is likely to ...
Objective: Cadherin-related 23 (CDH23) gene encodes a cell�cell adhesion protein which is required...
*<p>average of 500, 1000, 2000 and 4000 Hz.</p>**<p>average of 125, 250, and 500 Hz.</p>***<p>averag...
<p>(A): Pedigree of family LD-101 with hearing loss. This pedigree demonstrates nonsyndromic hearing...
<p>All three siblings (SNUH23–98, -99 and-52) exhibited partial deafness with preservation of signif...
<p><b>A<sup>I</sup></b>, Pedigree of the Qatari family carrying the p.*2625Gluext*11 mutation in <i>...
<p>(A) Pedigree of a large Danish family with moderate hearing impairment, with the proband indicate...
<p>(A) Pedigree of the family in which the <i>DFNB88</i> locus was mapped. The filled symbols repres...
Screening for gene mutations in CDH23, which has many exons, has lagged even though it is likely to ...
<p>(A, B) Squares and circles denote male and female family members, respectively. Filled symbols re...
<p>A. Patients with hearing loss caused by a c.235delC mutation (excluding patients with a p.V37I mu...
All in-text references underlined in blue are linked to publications on ResearchGate, letting you ac...
Nonsyndromic hearing loss has been shown to have high genetic heterogeneity. In this report, we aime...
<p>Pedigrees, mutations, and audiograms of the patients with compound heterozygous <i>CDH23</i> muta...
<p>Pedigrees, mutations, and audiograms of the patients with homozygous <i>CDH23</i> mutations.</p
Screening for gene mutations in CDH23, which has many exons, has lagged even though it is likely to ...
Objective: Cadherin-related 23 (CDH23) gene encodes a cell�cell adhesion protein which is required...
*<p>average of 500, 1000, 2000 and 4000 Hz.</p>**<p>average of 125, 250, and 500 Hz.</p>***<p>averag...
<p>(A): Pedigree of family LD-101 with hearing loss. This pedigree demonstrates nonsyndromic hearing...
<p>All three siblings (SNUH23–98, -99 and-52) exhibited partial deafness with preservation of signif...
<p><b>A<sup>I</sup></b>, Pedigree of the Qatari family carrying the p.*2625Gluext*11 mutation in <i>...
<p>(A) Pedigree of a large Danish family with moderate hearing impairment, with the proband indicate...
<p>(A) Pedigree of the family in which the <i>DFNB88</i> locus was mapped. The filled symbols repres...
Screening for gene mutations in CDH23, which has many exons, has lagged even though it is likely to ...
<p>(A, B) Squares and circles denote male and female family members, respectively. Filled symbols re...
<p>A. Patients with hearing loss caused by a c.235delC mutation (excluding patients with a p.V37I mu...
All in-text references underlined in blue are linked to publications on ResearchGate, letting you ac...
Nonsyndromic hearing loss has been shown to have high genetic heterogeneity. In this report, we aime...