Michael Hildebrand
University of Melbourne
104 papers found
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Genetic male infertility and mutation of CATSPER ion channels
Download from www.nature.commiRNA Mutations are Not a Common Cause of Deafness
Download from www.ncbi.nlm.nih.govVariable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation
Download from www.ncbi.nlm.nih.govHuman Male Infertility Caused by Mutations in the CATSPER1 Channel Protein
Download from www.ncbi.nlm.nih.govMutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss
UploadA novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family
Download from www.ncbi.nlm.nih.govMutation in the COCH gene is associated with superior semicircular canal dehiscence
Download from www.ncbi.nlm.nih.govA catechol-O-methyltransferase that is essential for auditory function in mice and humans
Download from doi.orgAutoimmune Disease in a DFNA6/14/38 Family carrying a Novel Missense Mutation in WFS1
Download from www.ncbi.nlm.nih.govA novel splice site mutation in EYA4 causes DFNA10 hearing loss (Am J Med Genet 143(14): 1599–1604)
Download from onlinelibrary.wiley.comClinical aspects of hereditary hearing loss
UploadMolecular characterization of a novel X-linked syndrome involving developmental delay and deafness
UploadCochlear Implants for DFNA17 Deafness:
UploadGenetic aspects of hearing loss
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