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The Application of Clinical Genetics
|
September 9, 2015
1p36 deletion syndrome: an update
Valerie K Jordan, Hitisha P Zaveri, Daryl A Scott
American Journal of Medical Genetics. Part A
|
April 3, 2015
Duplication of HEY2 in cardiac and neurologic development
Valerie K Jordan, Jill A Rosenfeld, Seema R Lalani, et al.
Human Molecular Genetics
|
March 27, 2021
RERE deficiency contributes to the development of orofacial clefts in humans and mice
Bum Jun Kim, Hitisha P Zaveri, Peter N Kundert, et al.
Disease Models & Mechanisms
|
August 1, 2018
RERE deficiency leads to decreased expression of GATA4 and the development of ventricular septal defects
Bum Jun Kim, Hitisha P Zaveri, Valerie K Jordan, et al.
Human Molecular Genetics
|
March 31, 2023
SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of Wnt4 and Bmp2
Andrés Hernández-García, Katherine E Pendleton, Sangbae Kim, et al.
Circulation
|
January 9, 2014
Ryanodine receptor-mediated calcium leak drives progressive development of an atrial fibrillation substrate in a transgenic mouse model
Na Li, David Y Chiang, Sufen Wang, et al.
Journal of Cellular Physiology
|
March 11, 2024
Running a successful STEMM summer program: A week-by-week guide
Heather K Beasley, Zer Vue, Melanie R McReynolds, et al.
American Journal of Medical Genetics. Part A
|
March 5, 2015
FBN1 contributing to familial congenital diaphragmatic hernia
Tyler F Beck, Philippe M Campeau, Shalini N Jhangiani, et al.
Journal of Medical Genetics
|
August 24, 2016
Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONO
Daryl A Scott, Andres Hernandez-Garcia, Mahshid S Azamian, et al.
Human Molecular Genetics
|
April 5, 2018
The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia
Valerie K Jordan, Tyler F Beck, Andres Hernandez-Garcia, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
The Application of Clinical Genetics
|
September 9, 2015
1p36 deletion syndrome: an update
Valerie K Jordan, Hitisha P Zaveri, Daryl A Scott
American Journal of Medical Genetics. Part A
|
April 3, 2015
Duplication of HEY2 in cardiac and neurologic development
Valerie K Jordan, Jill A Rosenfeld, Seema R Lalani, et al.
Human Molecular Genetics
|
March 27, 2021
RERE deficiency contributes to the development of orofacial clefts in humans and mice
Bum Jun Kim, Hitisha P Zaveri, Peter N Kundert, et al.
Disease Models & Mechanisms
|
August 1, 2018
RERE deficiency leads to decreased expression of GATA4 and the development of ventricular septal defects
Bum Jun Kim, Hitisha P Zaveri, Valerie K Jordan, et al.
Human Molecular Genetics
|
March 31, 2023
SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of Wnt4 and Bmp2
Andrés Hernández-García, Katherine E Pendleton, Sangbae Kim, et al.
Circulation
|
January 9, 2014
Ryanodine receptor-mediated calcium leak drives progressive development of an atrial fibrillation substrate in a transgenic mouse model
Na Li, David Y Chiang, Sufen Wang, et al.
Journal of Cellular Physiology
|
March 11, 2024
Running a successful STEMM summer program: A week-by-week guide
Heather K Beasley, Zer Vue, Melanie R McReynolds, et al.
American Journal of Medical Genetics. Part A
|
March 5, 2015
FBN1 contributing to familial congenital diaphragmatic hernia
Tyler F Beck, Philippe M Campeau, Shalini N Jhangiani, et al.
Journal of Medical Genetics
|
August 24, 2016
Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONO
Daryl A Scott, Andres Hernandez-Garcia, Mahshid S Azamian, et al.
Human Molecular Genetics
|
April 5, 2018
The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia
Valerie K Jordan, Tyler F Beck, Andres Hernandez-Garcia, et al.
Page
of 2