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Pathogenic mutations in TULP1 responsible for retinitis pigmentosa identified in consanguineous familial cases. [electronic resource] by
- Ullah, Inayat
- Kabir, Firoz
- Iqbal, Muhammad
- Gottsch, Clare Brooks S
- Naeem, Muhammad Asif
- Assir, Muhammad Zaman
- Khan, Shaheen N
- Akram, Javed
- Riazuddin, Sheikh
- Ayyagari, Radha
- Hejtmancik, J Fielding
- Riazuddin, S Amer
Producer: 20180129
In:
Molecular vision vol. 22
Availability: No items available.
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17.
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Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial cases. [electronic resource] by
- Kabir, Firoz
- Ullah, Inayat
- Ali, Shahbaz
- Gottsch, Alexander D H
- Naeem, Muhammad Asif
- Assir, Muhammad Zaman
- Khan, Shaheen N
- Akram, Javed
- Riazuddin, Sheikh
- Ayyagari, Radha
- Hejtmancik, J Fielding
- Riazuddin, S Amer
Producer: 20180115
In:
Molecular vision vol. 22
Availability: No items available.
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18.
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Cardiovascular Autonomic Neuropathy and its Association with Cardiovascular and All-cause Mortality in Patients with End-stage Renal Disease. [electronic resource] by
- Bokhari, Syed Rizwan A
- Inayat, Faisal
- Jawa, Ali
- Virk, Hafeez Ul Hasan
- Awais, Muhammad
- Hussain, Nadeem
- Hassan, Ghias Ul
- Ahmad, Hafiz Ijaz
- Chaudhry, Hammad S
- Adil, Abdullah
- Haider, Ali
- Figueredo, Vincent M
- Rangaswami, Janani
- Assir, Muhammad Zaman Khan
Publication details: Cureus Aug 2018
In:
Cureus vol. 10
Availability: No items available.
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19.
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Bi-allelic Variants in METTL5 Cause Autosomal-Recessive Intellectual Disability and Microcephaly. [electronic resource] by
- Richard, Elodie M
- Polla, Daniel L
- Assir, Muhammad Zaman
- Contreras, Minerva
- Shahzad, Mohsin
- Khan, Asma A
- Razzaq, Attia
- Akram, Javed
- Tarar, Moazzam N
- Blanpied, Thomas A
- Ahmed, Zubair M
- Abou Jamra, Rami
- Wieczorek, Dagmar
- van Bokhoven, Hans
- Riazuddin, Sheikh
- Riazuddin, Saima
Producer: 20200402
In:
American journal of human genetics vol. 105
Availability: No items available.
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20.
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Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening. [electronic resource] by
- 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
Producer: 20170426
In:
Investigative ophthalmology & visual science vol. 58
Availability: No items available.
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