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Showing results (361-370 of 391) with videos related to

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Human Mutation|October 2, 2010
The clinical spectrum of missense mutations of the first aspartic acid of cbEGF-like domains in fibrillin-1 including a recessive familyYvonne Hilhorst-Hofstee, Marry E B Rijlaarsdam, Arthur J H A Scholte, et al.
Biological Psychiatry|February 21, 2017
Nalmefene Reduces Reward Anticipation in Alcohol Dependence: An Experimental Functional Magnetic Resonance Imaging StudyDarren R Quelch, Inge Mick, John McGonigle, et al.
Oncogene|February 2, 1999
Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clusteredB A van der Reijden, H G Dauwerse, R H Giles, et al.
Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|June 26, 2021
FACE-Q craniofacial module: Part 2 Psychometric properties of newly developed scales for children and young adults with facial conditionsAnne F Klassen, Charlene Rae, Wong Riff, et al.
The Journal of Clinical Endocrinology and Metabolism|March 17, 2005
Homozygous and heterozygous expression of a novel insulin-like growth factor-I mutationM J E Walenkamp, M Karperien, A M Pereira, et al.
Journal of the American Society of Nephrology : JASN|April 23, 2003
Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney diseaseRiccardo Magistroni, Ning He, Kairong Wang, et al.
Journal of Medical Genetics|May 23, 2001
Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigreeA Wagner, Y Hendriks, E J Meijers-Heijboer, et al.
Clinical Genetics|July 13, 2010
Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysisD L Smit, A R Mensenkamp, S Badeloe, et al.
Nature Genetics|March 20, 2012
Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndromeGijs W E Santen, Emmelien Aten, Yu Sun, et al.
Gastroenterology|July 6, 2004
Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillanceYvonne M C Hendriks, Anja Wagner, Hans Morreau, et al.
Pageof 40

Showing results (361-370 of 391) with videos related to

Sort By:
Pageof 40
Human Mutation|October 2, 2010
The clinical spectrum of missense mutations of the first aspartic acid of cbEGF-like domains in fibrillin-1 including a recessive familyYvonne Hilhorst-Hofstee, Marry E B Rijlaarsdam, Arthur J H A Scholte, et al.
Biological Psychiatry|February 21, 2017
Nalmefene Reduces Reward Anticipation in Alcohol Dependence: An Experimental Functional Magnetic Resonance Imaging StudyDarren R Quelch, Inge Mick, John McGonigle, et al.
Oncogene|February 2, 1999
Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clusteredB A van der Reijden, H G Dauwerse, R H Giles, et al.
Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|June 26, 2021
FACE-Q craniofacial module: Part 2 Psychometric properties of newly developed scales for children and young adults with facial conditionsAnne F Klassen, Charlene Rae, Wong Riff, et al.
The Journal of Clinical Endocrinology and Metabolism|March 17, 2005
Homozygous and heterozygous expression of a novel insulin-like growth factor-I mutationM J E Walenkamp, M Karperien, A M Pereira, et al.
Journal of the American Society of Nephrology : JASN|April 23, 2003
Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney diseaseRiccardo Magistroni, Ning He, Kairong Wang, et al.
Journal of Medical Genetics|May 23, 2001
Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigreeA Wagner, Y Hendriks, E J Meijers-Heijboer, et al.
Clinical Genetics|July 13, 2010
Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysisD L Smit, A R Mensenkamp, S Badeloe, et al.
Nature Genetics|March 20, 2012
Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndromeGijs W E Santen, Emmelien Aten, Yu Sun, et al.
Gastroenterology|July 6, 2004
Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillanceYvonne M C Hendriks, Anja Wagner, Hans Morreau, et al.
Pageof 40