Incidence of Rhegmatogenous Retinal Detachment (RRD) in a Tertiary Care Center of Pakistan

por Iqbal, Saad M, Iqbal, Kashif, Shahid, Arslan, Iqbal, Faisal, Rahman, Fawad U, Tahir, Mohammad J, Qazi, Zaheeruddin A, Raheem, Usama, Butt, Jawad B, Ahmed, Moiz
Publicado 2022

Mapping of a new locus associated with autosomal recessive congenital cataract to chromosome 3q

por Sabir, Namerah, Riazuddin, S. Amer, Butt, Tariq, Iqbal, Farheena, Nasir, Idrees A., Zafar, Ahmad U., Qazi, Zaheeruddin A., Butt, Nadeem H., Khan, Shaheen N., Husnain, Tayyab, Hejtmancik, J. Fielding, Riazuddin, Sheikh
Publicado 2010

Mapping of a novel locus associated with autosomal recessive congenital cataract to chromosome 8p

por Sabir, Namerah, Riazuddin, S. Amer, Kaul, Haiba, Iqbal, Farheena, Nasir, Idrees A., Zafar, Ahmad U., Qazi, Zaheeruddin A., Butt, Nadeem H., Khan, Shaheen N., Husnain, Tayyab, Hejtmancik, J. Fielding, Riazuddin, Sheikh
Publicado 2010

Splice-site mutations identified in PDE6A responsible for retinitis pigmentosa in consanguineous Pakistani families

por Khan, Shahid Y., Ali, Shahbaz, Naeem, Muhammad Asif, Khan, Shaheen N., Husnain, Tayyab, Butt, Nadeem H., Qazi, Zaheeruddin A., Akram, Javed, Riazuddin, Sheikh, Ayyagari, Radha, Hejtmancik, J. Fielding, Riazuddin, S. Amer
Publicado 2015

Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1

por Yasmeen, Afshan, Riazuddin, S. Amer, Kaul, Haiba, Mohsin, Sadia, Khan, Mohsin, Qazi, Zaheeruddin A., Nasir, Idrees A., Zafar, Ahmad U., Khan, Shaheen N., Husnain, Tayyab, Akram, Javed, Hejtmancik, J. Fielding, Riazuddin, Sheikh
Publicado 2010

Mutations in GRM6 identified in consanguineous Pakistani families with congenital stationary night blindness

por Naeem, Muhammad Asif, Gottsch, Alexander D. H., Ullah, Inayat, Khan, Shaheen N., Husnain, Tayyab, Butt, Nadeem H., Qazi, Zaheeruddin A., Akram, Javed, Riazuddin, Sheikh, Ayyagari, Radha, Hejtmancik, J. Fielding, Riazuddin, S. Amer
Publicado 2015

Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening

por Chen, Jianjun, Wang, Qiwei, Cabrera, Patricia E., Zhong, Zilin, Sun, Wenmin, Jiao, Xiaodong, Chen, Yabin, Govindarajan, Gowthaman, Naeem, Muhammad Asif, Khan, Shaheen N., Ali, Muhammad Hassaan, Assir, Muhammad Zaman, Rahman, Fawad Ur, Qazi, Zaheeruddin A., Riazuddin, Sheikh, Akram, Javed, Riazuddin, S. Amer, Hejtmancik, J. Fielding
Publicado 2017