Items where Author is "Makhdoom, Ehtisham ul Haq"

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Makhdoom, Ehtisham ul Haq and Anwar, Haseeb and Baig, Shahid Mahmood and Hussain, Ghulam (2021) Whole exome sequencing identifies a novel mutation in ASPM and ultra-rare mutation in CDK5RAP2 causing Primary microcephaly in consanguineous Pakistani families. Pakistan Journal of Medical Sciences, 38 (1). ISSN 1682-024X

This list was generated on Sat Nov 23 16:08:04 2024 UTC.