Molecular and clinical studies of X-linked deafness among Pakistani families
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Published in Journal of human genetics (01.07.2011)
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Direct sequencing of FAH gene in Pakistani tyrosinemia type 1 families reveals a novel mutation
Ijaz, Sadaqat, Zahoor, Muhammad Yasir, Imran, Muhammad, Afzal, Sibtain, Bhinder, Munir A., Ullah, Ihsan, Cheema, Huma Arshad, Ramzan, Khushnooda, Shehzad, Wasim
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Published in Journal of Pediatric Endocrinology & Metabolism (01.03.2016)
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Genetic analysis through OtoSeq of Pakistani families segregating prelingual hearing loss
Shahzad, Mohsin, Sivakumaran, Theru A, Qaiser, Tanveer A, Schultz, Julie M, Hussain, Zawar, Flanagan, Megan, Bhinder, Munir A, Kissell, Diane, Greinwald, Jr, John H, Khan, Shaheen N, Friedman, Thomas B, Zhang, Kejian, Riazuddin, Saima, Riazuddin, Sheikh, Ahmed, Zubair M
Published in Otolaryngology-head and neck surgery (01.09.2013)
Published in Otolaryngology-head and neck surgery (01.09.2013)
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