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Melissa A Dempsey

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American Journal of Medical Genetics. Part A|April 14, 2007
Mosaicism del(22)(q11.2q11.2)/dup(22)(q11.2q11.2) in a patient with features of 22q11.2 deletion syndromeMelissa A Dempsey, Stuart Schwartz, Darrel J Waggoner
American Journal of Medical Genetics. Part A|January 30, 2007
Two cases further delineating the Sakoda complexMelissa A Dempsey, Wilfredo Torres-Martinez, Laurence E Walsh
Movement Disorders : Official Journal of the Movement Disorder Society|April 27, 2011
Novel mutations in siblings with later-onset PLA2G6-associated neurodegeneration (PLAN)Matthew A Bower, Khalaf Bushara, Melissa A Dempsey, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2007
A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohortGirish V Putcha, Bassem A Bejjani, Stacey Bleoo, et al.
Human Mutation|March 8, 2012
Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathyJohann Böhm, Valérie Biancalana, Elizabeth T Dechene, 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|April 14, 2007
Mosaicism del(22)(q11.2q11.2)/dup(22)(q11.2q11.2) in a patient with features of 22q11.2 deletion syndromeMelissa A Dempsey, Stuart Schwartz, Darrel J Waggoner
American Journal of Medical Genetics. Part A|January 30, 2007
Two cases further delineating the Sakoda complexMelissa A Dempsey, Wilfredo Torres-Martinez, Laurence E Walsh
Movement Disorders : Official Journal of the Movement Disorder Society|April 27, 2011
Novel mutations in siblings with later-onset PLA2G6-associated neurodegeneration (PLAN)Matthew A Bower, Khalaf Bushara, Melissa A Dempsey, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2007
A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohortGirish V Putcha, Bassem A Bejjani, Stacey Bleoo, et al.
Human Mutation|March 8, 2012
Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathyJohann Böhm, Valérie Biancalana, Elizabeth T Dechene, et al.
Pageof 1