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Syed Irfan

Showing results (91-100 of 104) with videos related to

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Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|September 15, 2020
Pancreaticoduodenectomy: Outcomes of a complex surgical procedure from a developing countryAun Jamal, Osama Shakeel, Jibran Mohsin, et al.
The International Journal of Biochemistry & Cell Biology|July 18, 2018
Molecular and in silico analyses validates pathogenicity of homozygous mutations in the NPR2 gene underlying variable phenotypes of Acromesomelic dysplasia, type MaroteauxIrfanullah, Amir Zeb, Naila Shinwari, et al.
Iscience|December 16, 2025
Challenges and strategies in developing high-performance n-type polycrystalline SnSe thermoelectric materialsAdeel Abbas, Habib Khan, Ch Asad Abbas, et al.
African Health Sciences|January 4, 2019
Family physicians' utility of social media: a survey comparison among family medicine residents and physiciansKarim Syed Irfan, Irfan Farhana, Al Faris Eiad, et al.
Chemosphere|December 2, 2022
Photocatalytic degradation of industrial dye using hybrid filler impregnated poly-sulfone membrane and optimizing the catalytic performance using Box-Behnken designSadaf Ul Hassan, Sidra Shafique, Bushra Anees Palvasha, et al.
Journal of Medical Genetics|July 11, 2015
A homozygous missense variant in type I keratin KRT25 causes autosomal recessive woolly hairMuhammad Ansar, Syed Irfan Raza, Kwanghyuk Lee, et al.
Journal of Human Genetics|June 17, 2021
Correction: Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13Anushree Acharya, Syed Irfan Raza, Muhammad Zeeshan Anwar, et al.
Journal of Human Genetics|April 21, 2021
Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13Anushree Acharya, Syed Irfan Raza, Muhammad Zeeshan Anwar, et al.
Journal of Human Genetics|December 1, 2018
Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significanceKhurram Liaqat, Isabelle Schrauwen, Syed Irfan Raza, et al.
Journal of Dermatological Science|October 21, 2015
Genetic analysis of Xp22.3 micro-deletions in seventeen families segregating isolated form of X-linked ichthyosisRaja Hussain Ali, Sabba Mahmood, Syed Irfan Raza, et al.
Pageof 11

Showing results (91-100 of 104) with videos related to

Sort By:
Pageof 11
Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|September 15, 2020
Pancreaticoduodenectomy: Outcomes of a complex surgical procedure from a developing countryAun Jamal, Osama Shakeel, Jibran Mohsin, et al.
The International Journal of Biochemistry & Cell Biology|July 18, 2018
Molecular and in silico analyses validates pathogenicity of homozygous mutations in the NPR2 gene underlying variable phenotypes of Acromesomelic dysplasia, type MaroteauxIrfanullah, Amir Zeb, Naila Shinwari, et al.
Iscience|December 16, 2025
Challenges and strategies in developing high-performance n-type polycrystalline SnSe thermoelectric materialsAdeel Abbas, Habib Khan, Ch Asad Abbas, et al.
African Health Sciences|January 4, 2019
Family physicians' utility of social media: a survey comparison among family medicine residents and physiciansKarim Syed Irfan, Irfan Farhana, Al Faris Eiad, et al.
Chemosphere|December 2, 2022
Photocatalytic degradation of industrial dye using hybrid filler impregnated poly-sulfone membrane and optimizing the catalytic performance using Box-Behnken designSadaf Ul Hassan, Sidra Shafique, Bushra Anees Palvasha, et al.
Journal of Medical Genetics|July 11, 2015
A homozygous missense variant in type I keratin KRT25 causes autosomal recessive woolly hairMuhammad Ansar, Syed Irfan Raza, Kwanghyuk Lee, et al.
Journal of Human Genetics|June 17, 2021
Correction: Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13Anushree Acharya, Syed Irfan Raza, Muhammad Zeeshan Anwar, et al.
Journal of Human Genetics|April 21, 2021
Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13Anushree Acharya, Syed Irfan Raza, Muhammad Zeeshan Anwar, et al.
Journal of Human Genetics|December 1, 2018
Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significanceKhurram Liaqat, Isabelle Schrauwen, Syed Irfan Raza, et al.
Journal of Dermatological Science|October 21, 2015
Genetic analysis of Xp22.3 micro-deletions in seventeen families segregating isolated form of X-linked ichthyosisRaja Hussain Ali, Sabba Mahmood, Syed Irfan Raza, et al.
Pageof 11