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Hitisha P Zaveri

Showing results (1-10 of 11) with videos related to

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The Application of Clinical Genetics|September 9, 2015
1p36 deletion syndrome: an updateValerie K Jordan, Hitisha P Zaveri, Daryl A Scott
American Journal of Medical Genetics. Part A|June 15, 2011
Delineation of a less than 200 kb minimal deleted region for cardiac malformations on chromosome 7p22Elliott G Richards, Hitisha P Zaveri, Varina L Wolf, et al.
Development (Cambridge, England)|June 28, 2015
Stromal Fat4 acts non-autonomously with Dchs1/2 to restrict the nephron progenitor poolMazdak Bagherie-Lachidan, Antoine Reginensi, Qun Pan, et al.
Human Molecular Genetics|March 27, 2021
RERE deficiency contributes to the development of orofacial clefts in humans and miceBum 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 defectsBum Jun Kim, Hitisha P Zaveri, Valerie K Jordan, et al.
Plos One|March 29, 2013
Novel frem1-related mouse phenotypes and evidence of genetic interactions with gata4 and slit3Tyler F Beck, Oleg A Shchelochkov, Zhiyin Yu, 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 Bmp2Andrés Hernández-García, Katherine E Pendleton, Sangbae Kim, et al.
Plos One|March 2, 2013
An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletionsBum Jun Kim, Hitisha P Zaveri, Oleg A Shchelochkov, et al.
Plos One|January 24, 2014
Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36Hitisha P Zaveri, Tyler F Beck, Andrés Hernández-García, et al.
Human Molecular Genetics|December 11, 2012
Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and miceTyler F Beck, Danielle Veenma, Oleg A Shchelochkov, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
The Application of Clinical Genetics|September 9, 2015
1p36 deletion syndrome: an updateValerie K Jordan, Hitisha P Zaveri, Daryl A Scott
American Journal of Medical Genetics. Part A|June 15, 2011
Delineation of a less than 200 kb minimal deleted region for cardiac malformations on chromosome 7p22Elliott G Richards, Hitisha P Zaveri, Varina L Wolf, et al.
Development (Cambridge, England)|June 28, 2015
Stromal Fat4 acts non-autonomously with Dchs1/2 to restrict the nephron progenitor poolMazdak Bagherie-Lachidan, Antoine Reginensi, Qun Pan, et al.
Human Molecular Genetics|March 27, 2021
RERE deficiency contributes to the development of orofacial clefts in humans and miceBum 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 defectsBum Jun Kim, Hitisha P Zaveri, Valerie K Jordan, et al.
Plos One|March 29, 2013
Novel frem1-related mouse phenotypes and evidence of genetic interactions with gata4 and slit3Tyler F Beck, Oleg A Shchelochkov, Zhiyin Yu, 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 Bmp2Andrés Hernández-García, Katherine E Pendleton, Sangbae Kim, et al.
Plos One|March 2, 2013
An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletionsBum Jun Kim, Hitisha P Zaveri, Oleg A Shchelochkov, et al.
Plos One|January 24, 2014
Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36Hitisha P Zaveri, Tyler F Beck, Andrés Hernández-García, et al.
Human Molecular Genetics|December 11, 2012
Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and miceTyler F Beck, Danielle Veenma, Oleg A Shchelochkov, et al.
Pageof 2