Autosomal recessive primary microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum

Tekijä Mahmood, Saqib, Ahmad, Wasim, Hassan, Muhammad J
Julkaistu 2011

CtIP Mutations Cause Seckel and Jawad Syndromes

Tekijä Qvist, Per, Huertas, Pablo, Jimeno, Sonia, Nyegaard, Mette, Hassan, Muhammad J., Jackson, Stephen P., Børglum, Anders D.
Julkaistu 2011

Novel duplication mutation of the DYSF gene in a Pakistani family with Miyoshi Myopathy

Tekijä Ullah, Muhammad I., Ahmad, Arsalan, Žarković, Milena, Shah, Syed S., Nasir, Abdul, Mahmood, Saqib, Ahmad, Wasim, Hübner, Christian A., Hassan, Muhammad J.
Julkaisussa Saudi Med J (2017)

Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39

Tekijä Schultz, Julie M., Khan, Shaheen N., Ahmed, Zubair M., Riazuddin, Saima, Waryah, Ali M., Chhatre, Dhananjay, Starost, Matthew F., Ploplis, Barbara, Buckley, Stephanie, Velásquez, David, Kabra, Madhulika, Lee, Kwanghyuk, Hassan, Muhammad J., Ali, Ghazanfar, Ansar, Muhammad, Ghosh, Manju, Wilcox, Edward R., Ahmad, Wasim, Merlino, Glenn, Leal, Suzanne M., Riazuddin, Sheikh, Friedman, Thomas B., Morell, Robert J.
Julkaistu 2009