18 results on '"Griffith, Andrew J."'
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2. Vestibular phenotype‐genotype correlation in a cohort of 90 patients with Usher syndrome
3. Hearing loss associated with enlarged vestibular aqueduct and zero or one mutant allele ofSLC26A4
4. Atypical patterns of segregation of familial enlargement of the vestibular aqueduct
5. Vestibular Dysfunction in Patients with Enlarged Vestibular Aqueduct
6. Vestibular Dysfunction in Patients with Enlarged Vestibular Aqueduct
7. SLC26A4 genotype, but not cochlear radiologic structure, is correlated with hearing loss in ears with an enlarged vestibular aqueduct
8. R085: Mutations of TMC1 in Families Segregating Recessive Deafness
9. Nonsyndromic hearing loss DFNA10 and a novel mutation ofEYA4: Evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain
10. Disruption offibroblast growth factor receptor 3 signaling results in defects in cellular differentiation, neuronal patterning, and hearing impairment
11. Auditory mechanotransduction in the absence of functional myosin‐XVa
12. Cochleosaccular Dysplasia Associated With a Connexin 26 Mutation in Keratitis???Ichthyosis???Deafness Syndrome
13. Stickler syndrome: Clinical characteristics and diagnostic criteria
14. Otolaryngologic Markers for Early Diagnosis of Turner Syndrome
15. Auditory Manifestations of Keratitis-Ichthyosis-Deafness (KID) Syndrome
16. Familial mondini dysplasia
17. Familial Large Vestibular Aqueduct Syndrome
18. Disruption of fibroblast growth factor receptor 3 signaling results in defects in cellular differentiation, neuronal patterning, and hearing impairment.
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