Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Saif Al Obaisi"'
Autor:
Bushra Irum, Shahid Y Khan, Muhammad Ali, Muhammad Daud, Firoz Kabir, Bushra Rauf, Fareeha Fatima, Hira Iqbal, Arif O Khan, Saif Al Obaisi, Muhammad Asif Naeem, Idrees A Nasir, Shaheen N Khan, Tayyab Husnain, Sheikh Riazuddin, Javed Akram, Allen O Eghrari, S Amer Riazuddin
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0173719 (2017)
[This corrects the article DOI: 10.1371/journal.pone.0167562.].
Externí odkaz:
https://doaj.org/article/d8d95d370b8b4cb59899a0efcdf14b9d
Autor:
Bushra Irum, Shahid Y Khan, Muhammad Ali, Muhammad Daud, Firoz Kabir, Bushra Rauf, Fareeha Fatima, Hira Iqbal, Arif O Khan, Saif Al Obaisi, Muhammad Asif Naeem, Idrees A Nasir, Shaheen N Khan, Tayyab Husnain, Sheikh Riazuddin, Javed Akram, Allen O Eghrari, S Amer Riazuddin
Publikováno v:
PLoS ONE, Vol 11, Iss 12, p e0167562 (2016)
The aim of this study is to identify the molecular basis of autosomal recessive congenital cataracts (arCC) in a large consanguineous pedigree.All participating individuals underwent a detailed ophthalmic examination. Each patient's medical history,
Externí odkaz:
https://doaj.org/article/c9f4adf0b7e7473aba3081364ed4681f
Autor:
Bushra Irum, Shahid Y Khan, Muhammad Ali, Haiba Kaul, Firoz Kabir, Bushra Rauf, Fareeha Fatima, Raheela Nadeem, Arif O Khan, Saif Al Obaisi, Muhammad Asif Naeem, Idrees A Nasir, Shaheen N Khan, Tayyab Husnain, Sheikh Riazuddin, Javed Akram, Allen O Eghrari, S Amer Riazuddin
Publikováno v:
PLoS ONE, Vol 11, Iss 11, p e0162620 (2016)
To identify the molecular basis of non-syndromic autosomal recessive congenital cataracts (arCC) in a consanguineous family.All family members participating in the study received a comprehensive ophthalmic examination to determine their ocular phenot
Externí odkaz:
https://doaj.org/article/22aedd3823ee4215ad62eaf53586fee8
Autor:
S. Amer Riazuddin, Muhammad Naeem, Bushra Rauf, Sheikh Riazuddin, Muhammad Daud, Allen O. Eghrari, Shahid Y. Khan, Tayyab Husnain, Firoz Kabir, Saif Al Obaisi, Idrees Ahmad Nasir, Shaheen N. Khan, Bushra Irum, Fareeha Fatima, Arif O. Khan, Javed Akram, Hira Iqbal, Muhammad Ali
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0173719 (2017)
PLoS ONE
PLoS ONE
The aim of this study is to identify the molecular basis of autosomal recessive congenital cataracts (arCC) in a large consanguineous pedigree.All participating individuals underwent a detailed ophthalmic examination. Each patient's medical history,
Autor:
Firoz Kabir, Bushra Rauf, Shahid Y. Khan, Shaheen N. Khan, Arif O. Khan, Fareeha Fatima, Idrees Ahmad Nasir, S. Amer Riazuddin, Saif Al Obaisi, Muhammad Daud, Sheikh Riazuddin, Muhammad Ali, Hira Iqbal, Allen O. Eghrari, Bushra Irum, Tayyab Husnain, Muhammad Asif Naeem, Javed Akram
Publikováno v:
PLoS ONE
PLoS ONE, Vol 11, Iss 12, p e0167562 (2016)
PLoS ONE, Vol 11, Iss 12, p e0167562 (2016)
PURPOSE The aim of this study is to identify the molecular basis of autosomal recessive congenital cataracts (arCC) in a large consanguineous pedigree. METHODS All participating individuals underwent a detailed ophthalmic examination. Each patient's
Autor:
Tayyab Husnain, Muhammad Asif Naeem, Bushra Irum, Bushra Rauf, Javed Akram, Sheikh Riazuddin, Arif O. Khan, Firoz Kabir, Muhammad Ali, S. Amer Riazuddin, Allen O. Eghrari, Haiba Kaul, Shaheen N. Khan, Fareeha Fatima, Shahid Y. Khan, Raheela Nadeem, Idrees Ahmad Nasir, Saif Al Obaisi
Publikováno v:
PLoS ONE, Vol 11, Iss 11, p e0162620 (2016)
PLoS ONE
PLoS ONE
Purpose To identify the molecular basis of non-syndromic autosomal recessive congenital cataracts (arCC) in a consanguineous family. Methods All family members participating in the study received a comprehensive ophthalmic examination to determine th