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Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
November 18, 2009
WNT5A mutations in patients with autosomal dominant Robinow syndrome
Anthony D Person, Soraya Beiraghi, Christine M Sieben, et al.
Human Genetics
|
April 17, 2007
Intragenic deletion in the LARGE gene causes Walker-Warburg syndrome
Jeroen van Reeuwijk, Prabhjit K Grewal, Mustafa A M Salih, et al.
Plos Genetics
|
November 9, 2013
Human intellectual disability genes form conserved functional modules in Drosophila
Merel A W Oortveld, Shivakumar Keerthikumar, Martin Oti, et al.
European Journal of Pediatrics
|
October 17, 2014
Sequencing of the DKK1 gene in patients with anorectal malformations and hypospadias
Romy van de Putte, Charlotte H W Wijers, Ivo de Blaauw, et al.
Journal of Medical Genetics
|
February 28, 2012
Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defects
Marjolein H Willemsen, Lisenka E L Vissers, Michèl A A P Willemsen, et al.
Journal of Cardiac Failure
|
September 22, 2019
Metabolic Profiling Associates with Disease Severity in Nonischemic Dilated Cardiomyopathy
Job A J Verdonschot, Ping Wang, Marc Van Bilsen, et al.
American Journal of Human Genetics
|
July 11, 2006
Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndrome
Neil V Morgan, Louise A Brueton, Phillip Cox, et al.
Circulation. Heart Failure
|
May 11, 2022
Dynamic Ejection Fraction Trajectory in Patients With Dilated Cardiomyopathy With a Truncating Titin Variant
Michiel T H M Henkens, Sophie L V M Stroeks, Anne G Raafs, et al.
Ebiomedicine
|
May 20, 2023
Evolution of age-related mutation-driven clonal haematopoiesis over 20 years is associated with metabolic dysfunction in obesity
Johanna C Andersson-Assarsson, Rosanne C van Deuren, Felipe M Kristensson, et al.
Nature Genetics
|
November 16, 2010
A de novo paradigm for mental retardation
Lisenka E L M Vissers, Joep de Ligt, Christian Gilissen, et al.
Page
of 73
Search research articles
Search
Showing results (501-510 of 727) with videos related to
Sort By:
Page
of 73
Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
November 18, 2009
WNT5A mutations in patients with autosomal dominant Robinow syndrome
Anthony D Person, Soraya Beiraghi, Christine M Sieben, et al.
Human Genetics
|
April 17, 2007
Intragenic deletion in the LARGE gene causes Walker-Warburg syndrome
Jeroen van Reeuwijk, Prabhjit K Grewal, Mustafa A M Salih, et al.
Plos Genetics
|
November 9, 2013
Human intellectual disability genes form conserved functional modules in Drosophila
Merel A W Oortveld, Shivakumar Keerthikumar, Martin Oti, et al.
European Journal of Pediatrics
|
October 17, 2014
Sequencing of the DKK1 gene in patients with anorectal malformations and hypospadias
Romy van de Putte, Charlotte H W Wijers, Ivo de Blaauw, et al.
Journal of Medical Genetics
|
February 28, 2012
Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defects
Marjolein H Willemsen, Lisenka E L Vissers, Michèl A A P Willemsen, et al.
Journal of Cardiac Failure
|
September 22, 2019
Metabolic Profiling Associates with Disease Severity in Nonischemic Dilated Cardiomyopathy
Job A J Verdonschot, Ping Wang, Marc Van Bilsen, et al.
American Journal of Human Genetics
|
July 11, 2006
Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndrome
Neil V Morgan, Louise A Brueton, Phillip Cox, et al.
Circulation. Heart Failure
|
May 11, 2022
Dynamic Ejection Fraction Trajectory in Patients With Dilated Cardiomyopathy With a Truncating Titin Variant
Michiel T H M Henkens, Sophie L V M Stroeks, Anne G Raafs, et al.
Ebiomedicine
|
May 20, 2023
Evolution of age-related mutation-driven clonal haematopoiesis over 20 years is associated with metabolic dysfunction in obesity
Johanna C Andersson-Assarsson, Rosanne C van Deuren, Felipe M Kristensson, et al.
Nature Genetics
|
November 16, 2010
A de novo paradigm for mental retardation
Lisenka E L M Vissers, Joep de Ligt, Christian Gilissen, et al.
Page
of 73