Studies in a consanguineous family reveal a novel locus for stuttering on chromosome 16q

Por Raza, M. Hashim, Ali, Rana Amjad, Riazuddin, S., Drayna, Dennis
Publicado em 2011

Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2

Por Santos-Cortez, Regie Lyn P., Faridi, Rabia, Rehman, Atteeq U., Lee, Kwanghyuk, Ansar, Muhammad, Wang, Xin, Morell, Robert J., Isaacson, Rivka, Belyantseva, Inna A., Dai, Hang, Acharya, Anushree, Qaiser, Tanveer A., Muhammad, Dost, Ali, Rana Amjad, Shams, Sulaiman, Hassan, Muhammad Jawad, Shahzad, Shaheen, Raza, Syed Irfan, Bashir, Zil-e-Huma, Smith, Joshua D., Nickerson, Deborah A., Bamshad, Michael J., Riazuddin, Sheikh, Ahmad, Wasim, Friedman, Thomas B., Leal, Suzanne M.
Publicado no Am J Hum Genet (2016)