Jamshaid Mahmood Baig

Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies

A. Need, A. Pagnamenta, M. Bleda, 2021, Genetics in Medicine.

An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan

A. Noegel, S. Baig, P. Nürnberg, 2020, Molecular genetics & genomic medicine.

Prevention of β-Thalassemia in a Large Pakistani Family through Cascade Testing

S. Baig, M. Aslam, M. Rasool, 2008, Public Health Genomics.

Prenatal diagnosis of β‐thalassemia in Southern Punjab, Pakistan

S. Baig, M. Aslam, T. Zaman, 2006 .