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Amir Hayat

Showing results (11-20 of 21) with videos related to

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Clinical Dysmorphology|August 31, 2019
A novel missense variant in the BBS7 gene underlying Bardet-Biedl syndrome in a consanguineous Pakistani familyAmir Hayat, Atif Ahmad Khan, Abdur Rauf, et al.
American Journal of Nephrology|June 5, 2009
Effect of ethnicity on the progression of diabetic kidney disease independent of glycemic controlMoro O Salifu, Syed Shah, Muhammad H Iqbal, et al.
Frontiers in Pediatrics|September 27, 2019
Biallelic Missense Mutation in the <i>ECEL1</i> Underlies Distal Arthrogryposis Type 5 (DA5D)Muhammad Umair, Amjad Khan, Amir Hayat, et al.
Genomics|December 16, 2020
Chloroplast genome evolution in the Dracunculus clade (Aroideae, Araceae)Abdullah, Claudia L Henriquez, Furrukh Mehmood, et al.
Molecular Syndromology|June 16, 2023
Identification of a Novel Nonsense Variant in the <i>DLL3</i> Gene Underlying Spondylocostal Dysostosis in a Consanguineous Pakistani FamilyFeroz Khan, Abida Arshad, Asmat Ullah, et al.
Clinical Transplantation|February 12, 2009
Long-term outcomes of dual kidney transplantation-a single center experienceMoro O Salifu, Allen J Norin, Christine O'Mahony, et al.
Genetic Testing and Molecular Biomarkers|August 9, 2020
Sequence Variants in the <i>WNT10B</i> and <i>TP63</i> Genes Underlying Isolated Split-Hand/Split-Foot MalformationMuhammad Bilal, Amir Hayat, Muhammad Umair, et al.
Molecular Syndromology|December 13, 2021
Variants in the <i>PNPLA1</i> Gene in Families with Autosomal Recessive Congenital Ichthyosis Reveal Clinical SignificanceFarooq Ahmad, Ishtiaq Ahmed, Qamre Alam, et al.
American Journal of Nephrology|January 14, 2010
New-onset diabetes after hemodialysis initiation: impact on survivalMoro O Salifu, Kevin C Abbott, Serhat Aytug, et al.
European Journal of Medical Genetics|May 16, 2020
Biallelic variants in four genes underlying recessive osteogenesis imperfectaAmir Hayat, Shabir Hussain, Muhammad Bilal, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Clinical Dysmorphology|August 31, 2019
A novel missense variant in the BBS7 gene underlying Bardet-Biedl syndrome in a consanguineous Pakistani familyAmir Hayat, Atif Ahmad Khan, Abdur Rauf, et al.
American Journal of Nephrology|June 5, 2009
Effect of ethnicity on the progression of diabetic kidney disease independent of glycemic controlMoro O Salifu, Syed Shah, Muhammad H Iqbal, et al.
Frontiers in Pediatrics|September 27, 2019
Biallelic Missense Mutation in the <i>ECEL1</i> Underlies Distal Arthrogryposis Type 5 (DA5D)Muhammad Umair, Amjad Khan, Amir Hayat, et al.
Genomics|December 16, 2020
Chloroplast genome evolution in the Dracunculus clade (Aroideae, Araceae)Abdullah, Claudia L Henriquez, Furrukh Mehmood, et al.
Molecular Syndromology|June 16, 2023
Identification of a Novel Nonsense Variant in the <i>DLL3</i> Gene Underlying Spondylocostal Dysostosis in a Consanguineous Pakistani FamilyFeroz Khan, Abida Arshad, Asmat Ullah, et al.
Clinical Transplantation|February 12, 2009
Long-term outcomes of dual kidney transplantation-a single center experienceMoro O Salifu, Allen J Norin, Christine O'Mahony, et al.
Genetic Testing and Molecular Biomarkers|August 9, 2020
Sequence Variants in the <i>WNT10B</i> and <i>TP63</i> Genes Underlying Isolated Split-Hand/Split-Foot MalformationMuhammad Bilal, Amir Hayat, Muhammad Umair, et al.
Molecular Syndromology|December 13, 2021
Variants in the <i>PNPLA1</i> Gene in Families with Autosomal Recessive Congenital Ichthyosis Reveal Clinical SignificanceFarooq Ahmad, Ishtiaq Ahmed, Qamre Alam, et al.
American Journal of Nephrology|January 14, 2010
New-onset diabetes after hemodialysis initiation: impact on survivalMoro O Salifu, Kevin C Abbott, Serhat Aytug, et al.
European Journal of Medical Genetics|May 16, 2020
Biallelic variants in four genes underlying recessive osteogenesis imperfectaAmir Hayat, Shabir Hussain, Muhammad Bilal, et al.
Pageof 3