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Eric Seboun

Showing results (1-10 of 5) with videos related to

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American Journal of Medical Genetics. Part A|February 22, 2005
Amish brittle hair syndrome gene maps to 7p14.1Eric Seboun, Arnaud Lemainque, Charles E Jackson
Annals of Human Genetics|May 6, 2006
Myotilin is not the causative gene for vocal cord and pharyngeal weakness with distal myopathy (VCPDM)Sean M Garvey, Jan Senderek, Jacques S Beckmann, et al.
American Journal of Human Genetics|August 28, 2010
Mutations in DHDPSL are responsible for primary hyperoxaluria type IIIRuth Belostotsky, Eric Seboun, Gregory H Idelson, et al.
American Journal of Human Genetics|April 7, 2009
Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3Jan Senderek, Sean M Garvey, Michael Krieger, et al.
American Journal of Human Genetics|January 13, 2005
Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophyKazuhiko Nakabayashi, Daniela Amann, Yan Ren, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|February 22, 2005
Amish brittle hair syndrome gene maps to 7p14.1Eric Seboun, Arnaud Lemainque, Charles E Jackson
Annals of Human Genetics|May 6, 2006
Myotilin is not the causative gene for vocal cord and pharyngeal weakness with distal myopathy (VCPDM)Sean M Garvey, Jan Senderek, Jacques S Beckmann, et al.
American Journal of Human Genetics|August 28, 2010
Mutations in DHDPSL are responsible for primary hyperoxaluria type IIIRuth Belostotsky, Eric Seboun, Gregory H Idelson, et al.
American Journal of Human Genetics|April 7, 2009
Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3Jan Senderek, Sean M Garvey, Michael Krieger, et al.
American Journal of Human Genetics|January 13, 2005
Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophyKazuhiko Nakabayashi, Daniela Amann, Yan Ren, et al.
Pageof 1