J. Baig

Prenatal diagnosis of β‐thalassemia in Southern Punjab, Pakistan

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

Spectrum of beta-thalassemia mutations in various regions of Punjab and Islamabad, Pakistan: establishment of prenatal diagnosis.

S. Baig, H. Bokhari, M. Aslam, 2006, Haematologica.

Prenatal diagnosis of beta-thalassemia in Southern Punjab, Pakistan.

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

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.

A 24‐generation‐old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome

L. Eichinger, A. Noegel, S. Baig, 2021, Clinical genetics.

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.

Molecular characterization of mutations causing β -thalassemia in Faisalabad Pakistan using the amplification refractory mutation system (ARMS-PCR)

S. Baig, T. Zaman, F. Rabbi, 2005 .