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Thomas M Morgan

Showing results (21-30 of 33) with videos related to

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BMC Medical Genetics|October 1, 2011
Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndromeThomas M Morgan, John A House, Sharon Cresci, et al.
Annals of Internal Medicine|November 4, 2009
National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving HealthAlfred O Berg, Macaran A Baird, Jeffrey R Botkin, et al.
NIH Consensus and State-Of-The-Science Statements|September 2, 2009
National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health: August 24-26, 2009Alfred O Berg, Macaran A Baird, Jeffrey R Botkin, et al.
European Journal of Human Genetics : EJHG|May 1, 2014
Homozygous loss of DIAPH1 is a novel cause of microcephaly in humansA Gulhan Ercan-Sencicek, Samira Jambi, Daniel Franjic, et al.
American Journal of Human Genetics|January 9, 2008
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disordersBetul Bakkaloglu, Brian J O'Roak, Angeliki Louvi, et al.
Molecular Cell|September 15, 2015
USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental DisorderYi-Heng Hao, Michael D Fountain, Klementina Fon Tacer, et al.
Science (New York, N.Y.)|October 15, 2005
Sequence variants in SLITRK1 are associated with Tourette's syndromeJesse F Abelson, Kenneth Y Kwan, Brian J O'Roak, et al.
American Journal of Human Genetics|May 2, 2017
Duplicated Enhancer Region Increases Expression of CTSB and Segregates with Keratolytic Winter Erythema in South African and Norwegian FamiliesThandiswa Ngcungcu, Martin Oti, Jan C Sitek, et al.
The New England Journal of Medicine|May 7, 2010
L-histidine decarboxylase and Tourette's syndromeA Gulhan Ercan-Sencicek, Althea A Stillman, Ananda K Ghosh, et al.
Journal of Medical Genetics|December 7, 2014
Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromesRobert B Hufnagel, Gavin Arno, Nichole D Hein, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
BMC Medical Genetics|October 1, 2011
Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndromeThomas M Morgan, John A House, Sharon Cresci, et al.
Annals of Internal Medicine|November 4, 2009
National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving HealthAlfred O Berg, Macaran A Baird, Jeffrey R Botkin, et al.
NIH Consensus and State-Of-The-Science Statements|September 2, 2009
National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health: August 24-26, 2009Alfred O Berg, Macaran A Baird, Jeffrey R Botkin, et al.
European Journal of Human Genetics : EJHG|May 1, 2014
Homozygous loss of DIAPH1 is a novel cause of microcephaly in humansA Gulhan Ercan-Sencicek, Samira Jambi, Daniel Franjic, et al.
American Journal of Human Genetics|January 9, 2008
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disordersBetul Bakkaloglu, Brian J O'Roak, Angeliki Louvi, et al.
Molecular Cell|September 15, 2015
USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental DisorderYi-Heng Hao, Michael D Fountain, Klementina Fon Tacer, et al.
Science (New York, N.Y.)|October 15, 2005
Sequence variants in SLITRK1 are associated with Tourette's syndromeJesse F Abelson, Kenneth Y Kwan, Brian J O'Roak, et al.
American Journal of Human Genetics|May 2, 2017
Duplicated Enhancer Region Increases Expression of CTSB and Segregates with Keratolytic Winter Erythema in South African and Norwegian FamiliesThandiswa Ngcungcu, Martin Oti, Jan C Sitek, et al.
The New England Journal of Medicine|May 7, 2010
L-histidine decarboxylase and Tourette's syndromeA Gulhan Ercan-Sencicek, Althea A Stillman, Ananda K Ghosh, et al.
Journal of Medical Genetics|December 7, 2014
Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromesRobert B Hufnagel, Gavin Arno, Nichole D Hein, et al.
Pageof 4