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Nicola C Ho

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

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American Journal of Medical Genetics. Part A|March 26, 2003
Famous people and genetic disorders: from monarchs to geniuses--a portrait of their genetic illnessesNicola C Ho, Susan S Park, Kevin D Maragh, et al.
BMC Neurology|July 4, 2003
Clinico-pathogenetic findings and management of chondrodystrophic myotonia (Schwartz-Jampel syndrome): a case reportNicola C Ho, Stacey Sandusky, Victor Madike, et al.
Genomics|February 6, 2002
Gene expression profile of human bone marrow stromal cells: high-throughput expressed sequence tag sequencing analysisLibin Jia, Marian F Young, John Powell, et al.
American Journal of Medical Genetics. Part A|October 16, 2004
Living with achondroplasia: quality of life evaluation following cervico-medullary decompressionNicola C Ho, Michael Guarnieri, Larry J Brant, et al.
American Journal of Human Genetics|April 10, 2002
Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasiaEri Arikawa-Hirasawa, Alexander H Le, Ichizo Nishino, 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|March 26, 2003
Famous people and genetic disorders: from monarchs to geniuses--a portrait of their genetic illnessesNicola C Ho, Susan S Park, Kevin D Maragh, et al.
BMC Neurology|July 4, 2003
Clinico-pathogenetic findings and management of chondrodystrophic myotonia (Schwartz-Jampel syndrome): a case reportNicola C Ho, Stacey Sandusky, Victor Madike, et al.
Genomics|February 6, 2002
Gene expression profile of human bone marrow stromal cells: high-throughput expressed sequence tag sequencing analysisLibin Jia, Marian F Young, John Powell, et al.
American Journal of Medical Genetics. Part A|October 16, 2004
Living with achondroplasia: quality of life evaluation following cervico-medullary decompressionNicola C Ho, Michael Guarnieri, Larry J Brant, et al.
American Journal of Human Genetics|April 10, 2002
Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasiaEri Arikawa-Hirasawa, Alexander H Le, Ichizo Nishino, et al.
Pageof 1