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Showing results (371-380 of 391) with videos related to

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Journal of Clinical Psychopharmacology|November 6, 2019
Effects of Pharmacogenetic Screening for CYP2D6 Among Elderly Starting Therapy With Nortriptyline or Venlafaxine: A Pragmatic Randomized Controlled Trial (CYSCE Trial)Jurjen van der Schans, Eelko Hak, Maarten Postma, et al.
Hormone Research|September 29, 2004
Genotype-phenotype correlation in patients suspected of having Sotos syndromeLonneke de Boer, Sarina G Kant, Marcel Karperien, et al.
Nature Genetics|December 7, 2010
Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndromeJohannes G Dauwerse, Jill Dixon, Saskia Seland, et al.
American Journal of Human Genetics|February 1, 1993
Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3M H Breuning, H G Dauwerse, G Fugazza, et al.
European Journal of Human Genetics : EJHG|September 26, 2013
Copy number variants in patients with short statureHermine A van Duyvenvoorde, Julian C Lui, Sarina G Kant, et al.
Journal of the American Society of Nephrology : JASN|July 10, 2010
Genetic variation of DKK3 may modify renal disease severity in ADPKDMichelle Liu, Sally Shi, Sean Senthilnathan, et al.
American Journal of Human Genetics|February 11, 1999
Molecular analysis of SALL1 mutations in Townes-Brocks syndromeJ Kohlhase, P E Taschner, P Burfeind, et al.
Human Genetics|September 12, 2000
Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13M Takahashi, E Rapley, P J Biggs, et al.
Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|July 18, 2021
FACE-Q Craniofacial Module: Part 1 validation of CLEFT-Q scales for use in children and young adults with facial conditionsAnne F Klassen, Charlene Rae, Karen Wy Wong Riff, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|September 3, 2017
A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defectsI H M van der Linde, Y L Hiemstra, R Bökenkamp, et al.
Pageof 40

Showing results (371-380 of 391) with videos related to

Sort By:
Pageof 40
Journal of Clinical Psychopharmacology|November 6, 2019
Effects of Pharmacogenetic Screening for CYP2D6 Among Elderly Starting Therapy With Nortriptyline or Venlafaxine: A Pragmatic Randomized Controlled Trial (CYSCE Trial)Jurjen van der Schans, Eelko Hak, Maarten Postma, et al.
Hormone Research|September 29, 2004
Genotype-phenotype correlation in patients suspected of having Sotos syndromeLonneke de Boer, Sarina G Kant, Marcel Karperien, et al.
Nature Genetics|December 7, 2010
Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndromeJohannes G Dauwerse, Jill Dixon, Saskia Seland, et al.
American Journal of Human Genetics|February 1, 1993
Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3M H Breuning, H G Dauwerse, G Fugazza, et al.
European Journal of Human Genetics : EJHG|September 26, 2013
Copy number variants in patients with short statureHermine A van Duyvenvoorde, Julian C Lui, Sarina G Kant, et al.
Journal of the American Society of Nephrology : JASN|July 10, 2010
Genetic variation of DKK3 may modify renal disease severity in ADPKDMichelle Liu, Sally Shi, Sean Senthilnathan, et al.
American Journal of Human Genetics|February 11, 1999
Molecular analysis of SALL1 mutations in Townes-Brocks syndromeJ Kohlhase, P E Taschner, P Burfeind, et al.
Human Genetics|September 12, 2000
Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13M Takahashi, E Rapley, P J Biggs, et al.
Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|July 18, 2021
FACE-Q Craniofacial Module: Part 1 validation of CLEFT-Q scales for use in children and young adults with facial conditionsAnne F Klassen, Charlene Rae, Karen Wy Wong Riff, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|September 3, 2017
A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defectsI H M van der Linde, Y L Hiemstra, R Bökenkamp, et al.
Pageof 40