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Movement Disorders : Official Journal of the Movement Disorder Society
|
August 19, 2005
Brisk deep-tendon reflexes as a distinctive phenotype in an Argentinean spinocerebellar ataxia type 2 pedigree
Alberto L Rosa, Irma Molina, Valeria Kowaljow, et al.
American Journal of Human Genetics
|
November 13, 2002
myotilin Mutation found in second pedigree with LGMD1A
Michael A Hauser, Cecilia B Conde, Valeria Kowaljow, et al.
Neuromuscular Disorders : NMD
|
June 26, 2007
The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein
Valeria Kowaljow, Aline Marcowycz, Eugénie Ansseau, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 3) with videos related to
Sort By:
Page
of 1
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 19, 2005
Brisk deep-tendon reflexes as a distinctive phenotype in an Argentinean spinocerebellar ataxia type 2 pedigree
Alberto L Rosa, Irma Molina, Valeria Kowaljow, et al.
American Journal of Human Genetics
|
November 13, 2002
myotilin Mutation found in second pedigree with LGMD1A
Michael A Hauser, Cecilia B Conde, Valeria Kowaljow, et al.
Neuromuscular Disorders : NMD
|
June 26, 2007
The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein
Valeria Kowaljow, Aline Marcowycz, Eugénie Ansseau, et al.
Page
of 1