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Microbiological Research|July 21, 2023
RNA-Seq analysis of mung bean (Vigna radiata L.) roots shows differential gene expression and predicts regulatory pathways responding to taxonomically different rhizobiaSughra Hakim, Asma Imran, Muhammad Sajid Hussain, et al.Cells|February 25, 2023
Congenital Microcephaly: A Debate on Diagnostic Challenges and Etiological Paradigm of the Shift from Isolated/Non-Syndromic to Syndromic MicrocephalyMaria Asif, Uzma Abdullah, Peter Nürnberg, et al.Journal of Human Genetics|March 2, 2023
Recurrence mutation in RBBP8 gene causing non-syndromic autosomal recessive primary microcephaly; geometric simulation approach for insight into predicted computational modelsTahira Batool, Saba Irshad, Muhammad Riaz, et al.Genes|May 4, 2026
Clinical and Molecular Characterization of Pakistani Mucopolysaccharidosis Families with SGSH and GALNS DeficienciesFarheen Nasir Awan, Shumaila Zulfiqar, Liza Eiman, et al.Human Genetics|December 2, 2015
A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani familySandra Szczepanski, Muhammad Sajid Hussain, Ilknur Sur, et al.American Journal of Medical Genetics. Part A|December 16, 2021
A novel missense variant of SCN4A co-segregates with congenital essential tremor in a consanguineous Kurdish familyMaria Asif, Ionut Dragos Mocanu, Uzma Abdullah, et al.Molecular Biology Reports|January 15, 2024
Investigating the effects of a single ASPM variant (c.8508_8509) on brain architecture among siblings in a consanguineous Pakistani familyKomal Aslam, Aysha Saeed, Iffat Jamil, et al.European Journal of Human Genetics : EJHG|January 14, 2010
Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRSMuhammad Farooq, Jesper T Troelsen, Mette Boyd, et al.American Journal of Human Genetics|April 24, 2012
A truncating mutation of CEP135 causes primary microcephaly and disturbed centrosomal functionMuhammad Sajid Hussain, Shahid Mahmood Baig, Sascha Neumann, et al.American Journal of Medical Genetics. Part A|April 9, 2009
Compound heterozygous ASPM mutations in Pakistani MCPH familiesFarooq Muhammad, Shahid Mahmood Baig, Lars Hansen, et al.Pageof 4