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D Lancet

Showing results (101-110 of 110) with videos related to

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Clinical Genetics|October 23, 2014
Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndromeD Oz-Levi, B Weiss, A Lahad, et al.
Current Topics in Developmental Biology|January 1, 1980
Complete primary structure of human histocompatibility antigen HLA-B7: evolutionary and functional implicationsJ L Strominger, V H Engelhard, B C Guild, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 3, 2017
Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavinG Heimer, E Eyal, X Zhu, et al.
Clinical Genetics|April 5, 2016
A role for TENM1 mutations in congenital general anosmiaA Alkelai, T Olender, R Haffner-Krausz, et al.
Genomics|October 15, 1997
Guidelines for human gene nomenclature (1997). HUGO Nomenclature CommitteeJ A White, P J McAlpine, S Antonarakis, 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.
Clinical Genetics|July 4, 2015
SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosumG Heimer, D Marek-Yagel, E Eyal, 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.
Pharmacogenetics|August 1, 1997
The UDP glycosyltransferase gene superfamily: recommended nomenclature update based on evolutionary divergenceP I Mackenzie, I S Owens, B Burchell, et al.
Nature|March 10, 2001
Initial sequencing and analysis of the human genomeE S Lander, L M Linton, B Birren, et al.
Pageof 11

Showing results (101-110 of 110) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 110 results.
Clinical Genetics|October 23, 2014
Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndromeD Oz-Levi, B Weiss, A Lahad, et al.
Current Topics in Developmental Biology|January 1, 1980
Complete primary structure of human histocompatibility antigen HLA-B7: evolutionary and functional implicationsJ L Strominger, V H Engelhard, B C Guild, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 3, 2017
Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavinG Heimer, E Eyal, X Zhu, et al.
Clinical Genetics|April 5, 2016
A role for TENM1 mutations in congenital general anosmiaA Alkelai, T Olender, R Haffner-Krausz, et al.
Genomics|October 15, 1997
Guidelines for human gene nomenclature (1997). HUGO Nomenclature CommitteeJ A White, P J McAlpine, S Antonarakis, 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.
Clinical Genetics|July 4, 2015
SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosumG Heimer, D Marek-Yagel, E Eyal, 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.
Pharmacogenetics|August 1, 1997
The UDP glycosyltransferase gene superfamily: recommended nomenclature update based on evolutionary divergenceP I Mackenzie, I S Owens, B Burchell, et al.
Nature|March 10, 2001
Initial sequencing and analysis of the human genomeE S Lander, L M Linton, B Birren, et al.
Pageof 11