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Muhammad Ansar

Showing results (131-140 of 191) with videos related to

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European Journal of Human Genetics : EJHG|December 24, 2015
Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disabilityMuhammad Ansar, Abid Jan, Regie Lyn P Santos-Cortez, et al.
International Journal of Dermatology|November 19, 2015
Novel mutations in the genes TGM1 and ALOXE3 underlying autosomal recessive congenital ichthyosisRahim Ullah, Muhammad Ansar, Zaka Ullah Durrani, et al.
Genes|February 25, 2023
Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani PedigreesAli Raza Rao, Aamir Nazir, Samina Imtiaz, et al.
NPJ Genomic Medicine|April 3, 2025
A comprehensive genetic landscape of inherited retinal diseases in a large Pakistani cohortMukhtar Ullah, Atta Ur Rehman, Mathieu Quinodoz, et al.
Peerj|August 3, 2019
Growth and development of soybean under changing light environments in relay intercropping systemMuhammad Ali Raza, Ling Yang Feng, Nasir Iqbal, et al.
Human Molecular Genetics|June 22, 2014
A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani familyMuzammil A Khan, Verena M Rupp, Meritxell Orpinell, et al.
Human Molecular Genetics|November 28, 2018
Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short statureMuhammad Ansar, Sohail Aziz Paracha, Alessandro Serretti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 25, 2023
Biallelic variants in NSUN6 cause an autosomal recessive neurodevelopmental disorderFrancesca Mattioli, Lina Worpenberg, Cai-Tao Li, et al.
Nature Genetics|October 5, 2010
WDR62 is associated with the spindle pole and is mutated in human microcephalyAdeline K Nicholas, Maryam Khurshid, Julie Désir, et al.
BMC Medical Genetics|February 17, 2016
Mitral regurgitation as a phenotypic manifestation of nonphotosensitive trichothiodystrophy due to a splice variant in MPLKIPKhadim Shah, Raja Hussain Ali, Muhammad Ansar, et al.
Pageof 20

Showing results (131-140 of 191) with videos related to

Sort By:
Pageof 20
European Journal of Human Genetics : EJHG|December 24, 2015
Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disabilityMuhammad Ansar, Abid Jan, Regie Lyn P Santos-Cortez, et al.
International Journal of Dermatology|November 19, 2015
Novel mutations in the genes TGM1 and ALOXE3 underlying autosomal recessive congenital ichthyosisRahim Ullah, Muhammad Ansar, Zaka Ullah Durrani, et al.
Genes|February 25, 2023
Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani PedigreesAli Raza Rao, Aamir Nazir, Samina Imtiaz, et al.
NPJ Genomic Medicine|April 3, 2025
A comprehensive genetic landscape of inherited retinal diseases in a large Pakistani cohortMukhtar Ullah, Atta Ur Rehman, Mathieu Quinodoz, et al.
Peerj|August 3, 2019
Growth and development of soybean under changing light environments in relay intercropping systemMuhammad Ali Raza, Ling Yang Feng, Nasir Iqbal, et al.
Human Molecular Genetics|June 22, 2014
A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani familyMuzammil A Khan, Verena M Rupp, Meritxell Orpinell, et al.
Human Molecular Genetics|November 28, 2018
Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short statureMuhammad Ansar, Sohail Aziz Paracha, Alessandro Serretti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 25, 2023
Biallelic variants in NSUN6 cause an autosomal recessive neurodevelopmental disorderFrancesca Mattioli, Lina Worpenberg, Cai-Tao Li, et al.
Nature Genetics|October 5, 2010
WDR62 is associated with the spindle pole and is mutated in human microcephalyAdeline K Nicholas, Maryam Khurshid, Julie Désir, et al.
BMC Medical Genetics|February 17, 2016
Mitral regurgitation as a phenotypic manifestation of nonphotosensitive trichothiodystrophy due to a splice variant in MPLKIPKhadim Shah, Raja Hussain Ali, Muhammad Ansar, et al.
Pageof 20