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International Journal of Molecular Sciences|October 14, 2022
An Insight into Molecular Targets of Breast Cancer Brain MetastasisMohammed Kaleem, Mahmood Hassan Dalhat, Lubna Azmi, et al.
Genes|April 23, 2022
Phenotype Expansion for Atypical Gaucher Disease Due to Homozygous Missense PSAP Variant in a Large Consanguineous Pakistani FamilyKhurram Liaqat, Shabir Hussain, Anushree Acharya, et al.
BMC Medical Genetics|August 25, 2019
Novel nonsense variants in SLURP1 and DSG1 cause palmoplantar keratoderma in Pakistani familiesAbida Akbar, Claire Prince, Chloe Payne, et al.
Molecules (Basel, Switzerland)|February 11, 2023
Nanomaterials-Based Novel Immune Strategies in Clinical Translation for Cancer TherapyShadma Wahab, Mohammed Ghazwani, Umme Hani, et al.
Clinical Genetics|June 13, 2023
Nonsense variant in a consanguineous family expands the phenotype of KPTN gene-related syndrome to include hearing impairmentKhurram Liaqat, Thashi Bharadwaj, Khadim Shah, et al.
Journal of Environmental Management|September 30, 2023
Advancements in technology and innovation for sustainable agriculture: Understanding and mitigating greenhouse gas emissions from agricultural soilsMuhammad Qayyum, Yanping Zhang, Mansi Wang, et al.
European Journal of Human Genetics : EJHG|September 29, 2005
Evidence for clinical and genetic heterogeneity of syndactyly type I: the phenotype of second and third toe syndactyly maps to chromosome 3p21.31Sajid Malik, Jörg Schott, Syed Wajahat Ali, et al.
3 Biotech|March 25, 2020
Box-Behnken supported development and validation of robust HPTLC method: an application in estimation of punarnavine in leaf, stem, and their callus of <i>Boerhavia diffusa</i> LinnWasim Ahmad, Ibraheem Husain, Niyaz Ahmad, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1-14q24.3 in large consanguineous kindred from PakistanMuhammad Ansar, Mohammad Amin ud Din, Muhammad Arshad, et al.
Archives of Medical Research|May 14, 2011
A novel deletion mutation in proteoglycan-4 underlies camptodactyly-arthropathy-coxa-vara-pericarditis syndrome in a consanguineous pakistani familySulman Basit, Zafar Iqbal, Masha Umicevic-Mirkov, et al.
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