15 results on '"Griffith, Andrew J."'
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2. CHD7 variants associated with hearing loss and enlargement of the vestibular aqueduct
3. Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss
4. Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria
5. Cochlear Pathomorphogenesis of Incomplete Partition Type II in Slc26a4-Null Mice
6. Systemic Fluorescent Gentamicin Enters Neonatal Mouse Hair Cells Predominantly Through Sensory Mechanoelectrical Transduction Channels
7. Tmc2 expression partially restores auditory function in a mouse model of DFNB7/B11 deafness caused by loss of Tmc1 function
8. Transmembrane channel-like (TMC) genes are required for auditory and vestibular mechanosensation
9. Hearing Loss is an Early Consequence of Npc1 Gene Deletion in the Mouse Model of Niemann–Pick Disease, Type C
10. The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3
11. Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorder
12. Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians
13. Knock-in Mouse Model for Resistance to Thyroid Hormone (RTH): An RTH Mutation in the Thyroid Hormone Receptor Beta Gene Disrupts Cochlear Morphogenesis
14. Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC
15. Nucleotide sequence and genomic structure analyses of the p70 subunit of the human Ku autoantigen: evidence for a family of genes encoding Ku (p70)-related polypeptides
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