M. Aslam

发表

Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene

M. Rafiq, P. John, W. Ahmad, 2005, Archives of Dermatological Research.

A novel locus for autosomal recessive form of hypotrichosis maps to chromosome 3q26.33–q27.3

S. Leal, M. Chahrour, W. Ahmad, 2004, Journal of Medical Genetics.

Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability

J. Vincent, G. Webersinke, C. Enzinger, 2014, Human molecular genetics.

A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontia

S. Baig, M. Rasool, Muhammad Tariq, 2008, Journal of Human Genetics.

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.

A missense point mutation in COL10A1 identified with whole-genome deep sequencing in a 7-generation Pakistan dwarf family

Xiong Yang, Shuhua Xu, Chao Zhang, 2017, Heredity.

WNT10A missense mutation associated with a complete Odonto-Onycho-Dermal Dysplasia syndrome

S. Baig, N. Dahl, M. Wajid, 2009, European Journal of Human Genetics.

Mutations in the genes for thyroglobulin and thyroid peroxidase cause thyroid dyshormonogenesis and autosomal-recessive intellectual disability

J. Vincent, M. Rafiq, Farooq Naeem, 2016, Journal of Human Genetics.

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

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

Compound heterozygous ASPM mutations in Pakistani MCPH families

N. Tommerup, H. Eiberg, P. Nürnberg, 2009, American journal of medical genetics. Part A.

A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31‐q22.3

S. Leal, M. Chahrour, W. Ahmad, 2005, American journal of medical genetics. Part A.