Search research articles
Contact Us
Filters
Showing results (1-10 of 7) with videos related to
Page
of 1
Sort By:
American Journal of Public Health
|
December 30, 2004
Community involvement in developing policies for genetic testing: assessing the interests and experiences of individuals affected by genetic conditions
Sarah E Gollust, Kira Apse, Barbara P Fuller, et al.
American Journal of Medical Genetics. Part A
|
May 13, 2006
Periventricular nodular heterotopia and Williams syndrome
Russell J Ferland, John N Gaitanis, Kira Apse, et al.
American Journal of Medical Genetics. Part A
|
May 12, 2005
EMX2-independent familial schizencephaly: clinical and genetic analyses
Ian Tietjen, Füsun Erdogan, Sophie Currier, et al.
Archives of Neurology
|
April 12, 2006
Cerebellar ataxia with progressive improvement
Jack W Tsao, Jason Neal, Kira Apse, et al.
American Journal of Medical Genetics. Part A
|
May 17, 2007
Comprehensive EMX2 genotyping of a large schizencephaly case series
Ian Tietjen, Adria Bodell, Kira Apse, et al.
American Journal of Medical Genetics. Part A
|
April 6, 2006
Bilateral periventricular heterotopias in an X-linked dominant transmission in a family with two affected males
Marion Gérard-Blanluet, Volney Sheen, Kalotina Machinis, et al.
Human Mutation
|
November 14, 2008
Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants of COH1
Wenke Seifert, Muriel Holder-Espinasse, Jirko Kühnisch, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
American Journal of Public Health
|
December 30, 2004
Community involvement in developing policies for genetic testing: assessing the interests and experiences of individuals affected by genetic conditions
Sarah E Gollust, Kira Apse, Barbara P Fuller, et al.
American Journal of Medical Genetics. Part A
|
May 13, 2006
Periventricular nodular heterotopia and Williams syndrome
Russell J Ferland, John N Gaitanis, Kira Apse, et al.
American Journal of Medical Genetics. Part A
|
May 12, 2005
EMX2-independent familial schizencephaly: clinical and genetic analyses
Ian Tietjen, Füsun Erdogan, Sophie Currier, et al.
Archives of Neurology
|
April 12, 2006
Cerebellar ataxia with progressive improvement
Jack W Tsao, Jason Neal, Kira Apse, et al.
American Journal of Medical Genetics. Part A
|
May 17, 2007
Comprehensive EMX2 genotyping of a large schizencephaly case series
Ian Tietjen, Adria Bodell, Kira Apse, et al.
American Journal of Medical Genetics. Part A
|
April 6, 2006
Bilateral periventricular heterotopias in an X-linked dominant transmission in a family with two affected males
Marion Gérard-Blanluet, Volney Sheen, Kalotina Machinis, et al.
Human Mutation
|
November 14, 2008
Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants of COH1
Wenke Seifert, Muriel Holder-Espinasse, Jirko Kühnisch, et al.
Page
of 1