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

por Mahmood, Saqib, Ahmad, Wasim, Hassan, Muhammad J
Publicado 2011

CtIP Mutations Cause Seckel and Jawad Syndromes

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

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

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

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

por 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.
Publicado 2009