Search results: Sage Journals

Restricted accessResearch articleFirst published November, 2008

Unique Transgenic Animal Model for Hereditary Hearing Loss

Maura Cosetti, David Culang, Sumankrishna Kotla [...]

Annals of Otology,Rhinology & Laryngology

Restricted accessResearch articleFirst published May, 1992

Malformation and Degeneration in the Inner Ear of MOS Transgenic Mice

Steven D. Rauch

Annals of Otology,Rhinology & Laryngology

Restricted accessResearch articleFirst published March, 1983

Mesodermal Induction Defect as a Possible Cause of Ear Malformations

Andrew R. Melnyk, Lester Weiss

Annals of Otology,Rhinology & Laryngology

Restricted accessResearch articleFirst published January, 2020

Inactivating Mutations in Exonuclease and Polymerase Domains in DNA Polymerase Delta Alter Sensitivities to Inhibitors of dNTP Synthesis

Jiaming Zhang, Deyin Hou, James Annis [...]

DNA and Cell Biology

Restricted accessResearch articleFirst published

Carrier Rates of the Ancestral Indian W24X Mutation in GJB2 in the General Gypsy Population and Individual Subisolates

Sonja Bouwer, Dora Angelicheva, David Chandler [...]

Genetic Testing and Molecular Biomarkers

Restricted accessOtherFirst published July, 2001

High Mitochondrial DNA T8993G Mutation (>90%) Without Typical Features of Leigh's and NARP Syndromes

Chang-Yong Tsao, Jerry R. Mendell, Dennis Bartholomew

Journal of Child Neurology

Restricted accessOtherFirst published May, 2007

Correlation Between mRNA Expression Level of the Mutant COL4A5 Gene and Phenotypes of XLAS Females

Yunfeng Wang, Hongwen Zhang, Jie Ding [...]

Experimental Biology and Medicine

Restricted accessBrief reportFirst published June, 2003

A Simple Method of Screening for the Common Connexin-26 Gene 35delG Mutation in Nonsyndromic Neurosensory Autosomal Recessive Deafness

Miguel Fernández-Burriel, Francisco Rodríguez-Quiñones

Genetic Testing and Molecular Biomarkers

Free accessResearch articleFirst published July, 2008

Pancreatic Metaplasia in the Gastro-achlorhydria in WTC- dfk Rat,a Potassium Channel Kcnq1 Mutant

M. Kuwamura, R. Okajima, J. Yamate [...]

Veterinary Pathology

Restricted accessResearch articleFirst published June, 2008

Genotyping for Cx26 and Cx30 Mutations in Cases with Congenital Hearing Loss

Neslihan Evirgen, Mustafa Solak, Sefa Dereköy [...]

Genetic Testing and Molecular Biomarkers

Restricted accessResearch articleFirst published November, 2008

Unique Transgenic Animal Model for Hereditary Hearing Loss

Maura Cosetti, David Culang, Sumankrishna Kotla [...]

Annals of Otology,Rhinology & Laryngology

Restricted accessResearch articleFirst published May, 1992

Malformation and Degeneration in the Inner Ear of MOS Transgenic Mice

Steven D. Rauch

Annals of Otology,Rhinology & Laryngology

Restricted accessResearch articleFirst published March, 1983

Mesodermal Induction Defect as a Possible Cause of Ear Malformations

Andrew R. Melnyk, Lester Weiss

Annals of Otology,Rhinology & Laryngology

Restricted accessResearch articleFirst published January, 2020

Inactivating Mutations in Exonuclease and Polymerase Domains in DNA Polymerase Delta Alter Sensitivities to Inhibitors of dNTP Synthesis

Jiaming Zhang, Deyin Hou, James Annis [...]

DNA and Cell Biology

Restricted accessResearch articleFirst published

Carrier Rates of the Ancestral Indian W24X Mutation in GJB2 in the General Gypsy Population and Individual Subisolates

Sonja Bouwer, Dora Angelicheva, David Chandler [...]

Genetic Testing and Molecular Biomarkers

Restricted accessOtherFirst published July, 2001

High Mitochondrial DNA T8993G Mutation (>90%) Without Typical Features of Leigh's and NARP Syndromes

Chang-Yong Tsao, Jerry R. Mendell, Dennis Bartholomew

Journal of Child Neurology

Restricted accessOtherFirst published May, 2007

Correlation Between mRNA Expression Level of the Mutant COL4A5 Gene and Phenotypes of XLAS Females

Yunfeng Wang, Hongwen Zhang, Jie Ding [...]

Experimental Biology and Medicine

Restricted accessBrief reportFirst published June, 2003

A Simple Method of Screening for the Common Connexin-26 Gene 35delG Mutation in Nonsyndromic Neurosensory Autosomal Recessive Deafness

Miguel Fernández-Burriel, Francisco Rodríguez-Quiñones

Genetic Testing and Molecular Biomarkers

Free accessResearch articleFirst published July, 2008

Pancreatic Metaplasia in the Gastro-achlorhydria in WTC- dfk Rat,a Potassium Channel Kcnq1 Mutant

M. Kuwamura, R. Okajima, J. Yamate [...]

Veterinary Pathology

Restricted accessResearch articleFirst published June, 2008

Genotyping for Cx26 and Cx30 Mutations in Cases with Congenital Hearing Loss

Neslihan Evirgen, Mustafa Solak, Sefa Dereköy [...]

Genetic Testing and Molecular Biomarkers