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Mental Retardation and Developmental Disabilities Research Reviews
|
June 5, 2003
The genetics of deafness
Walter E Nance
Science (New York, N.Y.)
|
September 5, 2002
Human reproductive cloning
Walter E Nance, John C Fletcher
American Journal of Human Genetics
|
April 14, 2004
Relevance of connexin deafness (DFNB1) to human evolution
Walter E Nance, Michael J Kearsey
The New England Journal of Medicine
|
May 19, 2006
Newborn hearing screening--a silent revolution
Cynthia C Morton, Walter E Nance
American Journal of Medical Genetics. Part A
|
September 16, 2004
Superficial siderosis: a potentially important cause of genetic as well as non-genetic deafness
Kelley M Dodson, Aristides Sismanis, Walter E Nance
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|
December 31, 2005
Importance of congenital cytomegalovirus infections as a cause for pre-lingual hearing loss
Walter E Nance, B Gail Lim, Kelley M Dodson
American Journal of Medical Genetics. Part A
|
May 15, 2007
Familial unilateral deafness and delayed endolymphatic hydrops
Kelley M Dodson, Tamio Kamei, Aristides Sismanis, et al.
American Journal of Medical Genetics. Part A
|
April 23, 2003
Chudley-McCullough syndrome: expanded phenotype and review of the literature
Katherine Oelrich Welch, Mustafa Tekin, Walter E Nance, et al.
Ear and Hearing
|
November 7, 2006
Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness? Penetrance of GJB2 deafness
Virginia W Norris, Kathleen S Arnos, Wendy D Hanks, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
March 26, 2013
The clinical and audiologic features of hearing loss due to mitochondrial mutations
Joshua C Yelverton, Kathleen Arnos, Xia-Juan Xia, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 26) with videos related to
Sort By:
Page
of 3
Mental Retardation and Developmental Disabilities Research Reviews
|
June 5, 2003
The genetics of deafness
Walter E Nance
Science (New York, N.Y.)
|
September 5, 2002
Human reproductive cloning
Walter E Nance, John C Fletcher
American Journal of Human Genetics
|
April 14, 2004
Relevance of connexin deafness (DFNB1) to human evolution
Walter E Nance, Michael J Kearsey
The New England Journal of Medicine
|
May 19, 2006
Newborn hearing screening--a silent revolution
Cynthia C Morton, Walter E Nance
American Journal of Medical Genetics. Part A
|
September 16, 2004
Superficial siderosis: a potentially important cause of genetic as well as non-genetic deafness
Kelley M Dodson, Aristides Sismanis, Walter E Nance
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|
December 31, 2005
Importance of congenital cytomegalovirus infections as a cause for pre-lingual hearing loss
Walter E Nance, B Gail Lim, Kelley M Dodson
American Journal of Medical Genetics. Part A
|
May 15, 2007
Familial unilateral deafness and delayed endolymphatic hydrops
Kelley M Dodson, Tamio Kamei, Aristides Sismanis, et al.
American Journal of Medical Genetics. Part A
|
April 23, 2003
Chudley-McCullough syndrome: expanded phenotype and review of the literature
Katherine Oelrich Welch, Mustafa Tekin, Walter E Nance, et al.
Ear and Hearing
|
November 7, 2006
Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness? Penetrance of GJB2 deafness
Virginia W Norris, Kathleen S Arnos, Wendy D Hanks, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
March 26, 2013
The clinical and audiologic features of hearing loss due to mitochondrial mutations
Joshua C Yelverton, Kathleen Arnos, Xia-Juan Xia, et al.
Page
of 3