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Human Mutation|April 24, 2001

Mucolipidosis type IV: novel MCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish populationR Bargal, N Avidan, T Olender, et al.

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.

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Showing results (21-30 of 24) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 24 results.

Human Mutation|April 24, 2001

Mucolipidosis type IV: novel MCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish populationR Bargal, N Avidan, T Olender, et al.

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.

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