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Muhammad Sajid

Showing results (631-640 of 645) with videos related to

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Annals of Neurology|September 12, 2017
Mutations of KIF14 cause primary microcephaly by impairing cytokinesisAbubakar Moawia, Ranad Shaheen, Sajida Rasool, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 18, 2022
Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signalingWilliam Dufour, Salem Alawbathani, Anne-Sophie Jourdain, et al.
Genes|June 2, 2021
Modifier Genes in Microcephaly: A Report on <i>WDR62</i>, <i>CEP63</i>, <i>RAD50</i> and <i>PCNT</i> Variants Exacerbating Disease Caused by Biallelic Mutations of <i>ASPM</i> and <i>CENPJ</i>Ehtisham Ul Haq Makhdoom, Syeda Seema Waseem, Maria Iqbal, et al.
American Journal of Human Genetics|December 3, 2014
Mutations in CKAP2L, the human homolog of the mouse Radmis gene, cause Filippi syndromeMuhammad Sajid Hussain, Agatino Battaglia, Sandra Szczepanski, et al.
Molecular Genetics & Genomic Medicine|July 18, 2020
An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from PakistanSajida Rasool, Jamshaid Mahmood Baig, Abubakar Moawia, et al.
Virology Journal|June 1, 2013
Genetic diversity of Newcastle disease virus in Pakistan: a countrywide perspectiveMuhammad Zubair Shabbir, Siamak Zohari, Tahir Yaqub, et al.
BMC Genomics|October 31, 2018
Integration of conventional and advanced molecular tools to track footprints of heterosis in cottonZareen Sarfraz, Muhammad Shahid Iqbal, Zhaoe Pan, et al.
Journal of Global Health|November 23, 2017
Understanding biological mechanisms underlying adverse birth outcomes in developing countries: protocol for a prospective cohort (AMANHI bio-banking) study, Abdullah H Baqui, Rasheda Khanam, et al.
Frontiers in Plant Science|June 7, 2021
GWAS Mediated Elucidation of Heterosis for Metric Traits in Cotton (<i>Gossypium hirsutum</i> L.) Across Multiple EnvironmentsZareen Sarfraz, Muhammad Shahid Iqbal, Xiaoli Geng, et al.
Clinical Genetics|July 16, 2021
A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndromeEmrah Kaygusuz, Arwa Ishaq A Khayyat, Uzma Abdullah, et al.
Pageof 65

Showing results (631-640 of 645) with videos related to

Sort By:
Pageof 65
Annals of Neurology|September 12, 2017
Mutations of KIF14 cause primary microcephaly by impairing cytokinesisAbubakar Moawia, Ranad Shaheen, Sajida Rasool, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 18, 2022
Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signalingWilliam Dufour, Salem Alawbathani, Anne-Sophie Jourdain, et al.
Genes|June 2, 2021
Modifier Genes in Microcephaly: A Report on <i>WDR62</i>, <i>CEP63</i>, <i>RAD50</i> and <i>PCNT</i> Variants Exacerbating Disease Caused by Biallelic Mutations of <i>ASPM</i> and <i>CENPJ</i>Ehtisham Ul Haq Makhdoom, Syeda Seema Waseem, Maria Iqbal, et al.
American Journal of Human Genetics|December 3, 2014
Mutations in CKAP2L, the human homolog of the mouse Radmis gene, cause Filippi syndromeMuhammad Sajid Hussain, Agatino Battaglia, Sandra Szczepanski, et al.
Molecular Genetics & Genomic Medicine|July 18, 2020
An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from PakistanSajida Rasool, Jamshaid Mahmood Baig, Abubakar Moawia, et al.
Virology Journal|June 1, 2013
Genetic diversity of Newcastle disease virus in Pakistan: a countrywide perspectiveMuhammad Zubair Shabbir, Siamak Zohari, Tahir Yaqub, et al.
BMC Genomics|October 31, 2018
Integration of conventional and advanced molecular tools to track footprints of heterosis in cottonZareen Sarfraz, Muhammad Shahid Iqbal, Zhaoe Pan, et al.
Journal of Global Health|November 23, 2017
Understanding biological mechanisms underlying adverse birth outcomes in developing countries: protocol for a prospective cohort (AMANHI bio-banking) study, Abdullah H Baqui, Rasheda Khanam, et al.
Frontiers in Plant Science|June 7, 2021
GWAS Mediated Elucidation of Heterosis for Metric Traits in Cotton (<i>Gossypium hirsutum</i> L.) Across Multiple EnvironmentsZareen Sarfraz, Muhammad Shahid Iqbal, Xiaoli Geng, et al.
Clinical Genetics|July 16, 2021
A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndromeEmrah Kaygusuz, Arwa Ishaq A Khayyat, Uzma Abdullah, et al.
Pageof 65