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R Monroe

Showing results (241-250 of 277) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 5, 2016
Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disabilityGlen R Monroe, Gerardus W Frederix, Sanne M C Savelberg, et al.
Plos One|November 18, 2014
A pooled analysis of body mass index and mortality among African AmericansSarah S Cohen, Yikyung Park, Lisa B Signorello, et al.
European Journal of Human Genetics : EJHG|August 18, 2016
Compound heterozygous NEK1 variants in two siblings with oral-facial-digital syndrome type II (Mohr syndrome)Glen R Monroe, Isabelle Fpm Kappen, Marijn F Stokman, et al.
American Journal of Epidemiology|July 4, 2013
Association of the FTO obesity risk variant rs8050136 with percentage of energy intake from fat in multiple racial/ethnic populations: the PAGE studySungshim Lani Park, Iona Cheng, Sarah A Pendergrass, et al.
American Journal of Human Genetics|September 13, 2016
De Novo Mutations in CHD4, an ATP-Dependent Chromatin Remodeler Gene, Cause an Intellectual Disability Syndrome with Distinctive DysmorphismsKarin Weiss, Paulien A Terhal, Lior Cohen, et al.
The New England Journal of Medicine|November 13, 2014
Monocarboxylate transporter 1 deficiency and ketone utilizationPeter M van Hasselt, Sacha Ferdinandusse, Glen R Monroe, et al.
The Journal of Clinical Investigation|February 14, 2017
Synaptic UNC13A protein variant causes increased neurotransmission and dyskinetic movement disorderNoa Lipstein, Nanda M Verhoeven-Duif, Francesco E Michelassi, et al.
Journal of Medical Genetics|October 23, 2015
MKS1 regulates ciliary INPP5E levels in Joubert syndromeGisela G Slaats, Christine R Isabella, Hester Y Kroes, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 18, 2018
Family History of Cancer and Risk of Biliary Tract Cancers: Results from the Biliary Tract Cancers Pooling ProjectAlison L Van Dyke, Margaret S Langhamer, Bin Zhu, et al.
Plos Genetics|February 6, 2013
Phenome-wide association study (PheWAS) for detection of pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) NetworkSarah A Pendergrass, Kristin Brown-Gentry, Scott Dudek, et al.
Pageof 28

Showing results (241-250 of 277) with videos related to

Sort By:
Pageof 28
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 5, 2016
Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disabilityGlen R Monroe, Gerardus W Frederix, Sanne M C Savelberg, et al.
Plos One|November 18, 2014
A pooled analysis of body mass index and mortality among African AmericansSarah S Cohen, Yikyung Park, Lisa B Signorello, et al.
European Journal of Human Genetics : EJHG|August 18, 2016
Compound heterozygous NEK1 variants in two siblings with oral-facial-digital syndrome type II (Mohr syndrome)Glen R Monroe, Isabelle Fpm Kappen, Marijn F Stokman, et al.
American Journal of Epidemiology|July 4, 2013
Association of the FTO obesity risk variant rs8050136 with percentage of energy intake from fat in multiple racial/ethnic populations: the PAGE studySungshim Lani Park, Iona Cheng, Sarah A Pendergrass, et al.
American Journal of Human Genetics|September 13, 2016
De Novo Mutations in CHD4, an ATP-Dependent Chromatin Remodeler Gene, Cause an Intellectual Disability Syndrome with Distinctive DysmorphismsKarin Weiss, Paulien A Terhal, Lior Cohen, et al.
The New England Journal of Medicine|November 13, 2014
Monocarboxylate transporter 1 deficiency and ketone utilizationPeter M van Hasselt, Sacha Ferdinandusse, Glen R Monroe, et al.
The Journal of Clinical Investigation|February 14, 2017
Synaptic UNC13A protein variant causes increased neurotransmission and dyskinetic movement disorderNoa Lipstein, Nanda M Verhoeven-Duif, Francesco E Michelassi, et al.
Journal of Medical Genetics|October 23, 2015
MKS1 regulates ciliary INPP5E levels in Joubert syndromeGisela G Slaats, Christine R Isabella, Hester Y Kroes, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 18, 2018
Family History of Cancer and Risk of Biliary Tract Cancers: Results from the Biliary Tract Cancers Pooling ProjectAlison L Van Dyke, Margaret S Langhamer, Bin Zhu, et al.
Plos Genetics|February 6, 2013
Phenome-wide association study (PheWAS) for detection of pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) NetworkSarah A Pendergrass, Kristin Brown-Gentry, Scott Dudek, et al.
Pageof 28