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Gene|December 11, 2012
Novel homozygous mutations in the genes ARL6 and BBS10 underlying Bardet-Biedl syndromeSaadullah Khan, Imran Ullah, Irfanullah, et al.Gene|November 12, 2013
Novel homozygous mutations in the WNT10B gene underlying autosomal recessive split hand/foot malformation in three consanguineous familiesAbdul Aziz, Irfanullah, Saadullah Khan, et al.Human Genetics|August 31, 2011
Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13.3-q21.2 and screening of the candidate genesUmm-e-Kalsoom, Sulman Basit, Syed Kamran-ul-Hassan Naqvi, et al.Journal of Neurogenetics|September 13, 2007
Novel protein-truncating mutations in the ASPM gene in families with autosomal recessive primary microcephalyAsma Gul, Muhammad Tariq, Muhammad Nasim Khan, et al.Journal of Dermatological Science|January 27, 2009
Novel missense mutations in lipase H (LIPH) gene causing autosomal recessive hypotrichosis (LAH2)Gul Naz, Bushra Khan, Ghazanfar Ali, et al.Scientific Reports|January 11, 2025
Intelligent skin disease prediction system using transfer learning and explainable artificial intelligenceSagheer Abbas, Fahad Ahmed, Wasim Ahmad Khan, et al.Molecular Biology Reports|October 28, 2023
Sequence variants in different genes underlying Bardet-Biedl syndrome in four consanguineous familiesAmjad Ali, Abdullah, Muhammad Bilal, et al.Journal of Human Genetics|August 11, 2006
A novel deletion mutation in CENPJ gene in a Pakistani family with autosomal recessive primary microcephalyAsma Gul, Muhammad Jawad Hassan, Sabir Hussain, et al.Journal of Cleaner Production|January 23, 2023
Determinants of CSR and green purchase intention: Mediating role of customer green psychology during COVID-19 pandemicWasim Ahmad, Rana Muhammad Sohail Jafar, Abdul Waheed, et al.Human Genetics|December 29, 2010
Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani familiesNaveed Wasif, Syed Kamran ul-Hassan Naqvi, Sulman Basit, et al.Pageof 34