*<p>average of 500, 1000, 2000 and 4000 Hz.</p>**<p>average of 125, 250, and 500 Hz.</p>***<p>average of 2000, 4000, and 8000 Hz.</p>****<p>found by newborn hearing screening.</p
CDH23 mutations have mostly been associated with prelingual severe-to-profound sensorineural hearing...
Item does not contain fulltextUsher syndrome type I is characterized by congenital hearing loss, ret...
<p>A. Patients with hearing loss caused by a c.235delC mutation (excluding patients with a p.V37I mu...
Screening for gene mutations in CDH23, which has many exons, has lagged even though it is likely to ...
<p>Pedigrees, mutations, and audiograms of the patients with compound heterozygous <i>CDH23</i> muta...
Screening for gene mutations in CDH23, which has many exons, has lagged even though it is likely to ...
<p>Audiogram: Right (red) and left (blue) ear hearing thresholds. Pedigree: Filled symbols represent...
All in-text references underlined in blue are linked to publications on ResearchGate, letting you ac...
<p>Note that the high frequency portion was already worsened, and the low frequency portion was dete...
<p>Pedigrees, mutations, and audiograms of the patients with homozygous <i>CDH23</i> mutations.</p
信州大学博士（医学）・学位論文・平成25年1月30日授与（乙第1154号）・宮川 麻衣子Screening for gene mutations in CDH23, which has many ex...
<p>Hearing levels of patients with the p.V37I/c.235delC compound heterozygous variation.</p
Usher syndrome type I is characterized by congenital hearing loss, retinitis pigmentosa (RP), and va...
Objective: Cadherin-related 23 (CDH23) gene encodes a cell�cell adhesion protein which is required...
Usher syndrome type I is characterized by congenital hearing loss, retinitis pigmentosa (RP), and va...
CDH23 mutations have mostly been associated with prelingual severe-to-profound sensorineural hearing...
Item does not contain fulltextUsher syndrome type I is characterized by congenital hearing loss, ret...
<p>A. Patients with hearing loss caused by a c.235delC mutation (excluding patients with a p.V37I mu...
Screening for gene mutations in CDH23, which has many exons, has lagged even though it is likely to ...
<p>Pedigrees, mutations, and audiograms of the patients with compound heterozygous <i>CDH23</i> muta...
Screening for gene mutations in CDH23, which has many exons, has lagged even though it is likely to ...
<p>Audiogram: Right (red) and left (blue) ear hearing thresholds. Pedigree: Filled symbols represent...
All in-text references underlined in blue are linked to publications on ResearchGate, letting you ac...
<p>Note that the high frequency portion was already worsened, and the low frequency portion was dete...
<p>Pedigrees, mutations, and audiograms of the patients with homozygous <i>CDH23</i> mutations.</p
信州大学博士（医学）・学位論文・平成25年1月30日授与（乙第1154号）・宮川 麻衣子Screening for gene mutations in CDH23, which has many ex...
<p>Hearing levels of patients with the p.V37I/c.235delC compound heterozygous variation.</p
Usher syndrome type I is characterized by congenital hearing loss, retinitis pigmentosa (RP), and va...
Objective: Cadherin-related 23 (CDH23) gene encodes a cell�cell adhesion protein which is required...
Usher syndrome type I is characterized by congenital hearing loss, retinitis pigmentosa (RP), and va...
CDH23 mutations have mostly been associated with prelingual severe-to-profound sensorineural hearing...
Item does not contain fulltextUsher syndrome type I is characterized by congenital hearing loss, ret...
<p>A. Patients with hearing loss caused by a c.235delC mutation (excluding patients with a p.V37I mu...
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