Myo15 function is distinct from Myo6 , Myo7a and pirouette genes in development of cochlear stereocilia

By Karolyi I. Jill  

Human Molecular Genetics, Vol. 12, Iss. 21, 2003-11 ,pp. : 2797-2805

Oxford University Press

Access to resources Recommend Favorite

A Novel de novo Mutation in CEACAM16 Associated with Postlingual Hearing Impairment

By  

Molecular Syndromology, Vol. 6, Iss. 4, 2015-0 ,pp. : 156-163

Karger

Access to resources Recommend Favorite

Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese

By Fukuoka Hisakuni   Kanda Yukihiko   Ohta Shuji   Usami Shin-ichi  

Journal of Human Genetics, Vol. 52, Iss. 6, 2007-06 ,pp. : 510-515

Springer Publishing Company

Access to resources Recommend Favorite

GRM7 variants confer susceptibility to age-related hearing impairment

By Friedman Rick A.   Van Laer Lut   Huentelman Matthew J.   Sheth Sonal S.   Van Eyken Els   Corneveaux Jason J.   Tembe Waibhav D.   Halperin Rebecca F.   Thorburn Ashley Q.   Thys Sofie   Bonneux Sarah   Fransen Erik   Huyghe Jeroen   Pyykk Ilmari   Cremers Cor W.R.J.   Kremer Hannie   Dhooge Ingeborg   Stephens Dafydd   Orzan Eva   Pfister Markus   Bille Michael   Parving Agnete   Sorri Martti   Van de Heyning Paul H.   Makmura Linna   Ohmen Jeffrey D.   Linthicum Frederick H.   Fayad Jose N.   Pearson John V.   Craig David W.   Stephan Dietrich A.   Van Camp Guy  

Human Molecular Genetics, Vol. 18, Iss. 4, 2009-02 ,pp. : 785-796

Oxford University Press

Access to resources Recommend Favorite

A deletion on Chromosome 4 cosegregates with the whirler deafness mutation: exclusion of as a candidate

By Paige Adam J.W.   Kiernan Brent W.   Varela Anabel   Rogers Michael J.C.   Hughes David   Steel Karen P.   Brown Steve D.M.  

Mammalian Genome, Vol. 11, Iss. 1, 2000-01 ,pp. : 51-57

Springer Publishing Company

Access to resources Recommend Favorite