USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1

por Jaworek, Thomas J., Bhatti, Rashid, Latief, Naureen, Khan, Shaheen N., Riazuddin, Saima, Ahmed, Zubair M
Publicado 2012

An Alteration in ELMOD3, an Arl2 GTPase-Activating Protein, Is Associated with Hearing Impairment in Humans

por Jaworek, Thomas J., Richard, Elodie M., Ivanova, Anna A., Giese, Arnaud P. J., Choo, Daniel I., Khan, Shaheen N., Riazuddin, Sheikh, Kahn, Richard A., Riazuddin, Saima
Publicado 2013

Molecular genetic studies and delineation of the oculocutaneous albinism phenotype in the Pakistani population

por Jaworek, Thomas J, Kausar, Tasleem, Bell, Shannon M, Tariq, Nabeela, Maqsood, Muhammad Imran, Sohail, Asma, Ali, Muhmmmad, Iqbal, Furhan, Rasool, Shafqat, Riazuddin, Saima, Shaikh, Rehan S, Ahmed, Zubair M
Publicado 2012