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Showing results (11-20 of 14) with videos related to

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Genomics|February 16, 2000
Sequence, structure, and evolution of a complete human olfactory receptor gene clusterG Glusman, A Sosinsky, E Ben-Asher, et al.
American Journal of Human Genetics|November 13, 2001
A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from IsraelH Lahat, E Pras, T Olender, et al.
Gene|February 17, 2001
Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1D Levanon, G Glusman, T Bangsow, et al.
Nature Genetics|August 31, 2001
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathyI Eisenberg, N Avidan, T Potikha, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Genomics|February 16, 2000
Sequence, structure, and evolution of a complete human olfactory receptor gene clusterG Glusman, A Sosinsky, E Ben-Asher, et al.
American Journal of Human Genetics|November 13, 2001
A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from IsraelH Lahat, E Pras, T Olender, et al.
Gene|February 17, 2001
Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1D Levanon, G Glusman, T Bangsow, et al.
Nature Genetics|August 31, 2001
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathyI Eisenberg, N Avidan, T Potikha, et al.
Pageof 2