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XPC gene mutations in families with xeroderma pigmentosum from Pakistan; prevalent founder effect
Ambreen Ijaz, Sulman Basit, Ajab Gul, Lilas Batool, Abrar Hussain, Sibtain Afzal, Khushnooda Ramzan, Jamil Ahmad, Abdul Wali
(2019)
Congenital anomalies
vol.
59
no.
1
pp.
18-21
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Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation
Asmat Ullah, Ajab Gul, Muhammad Umair, Irfanullah, Farooq Ahmad, Abdul Aziz, Abdul Wali, Wasim Ahmad
(2018)
Genetics and Molecular Biology
vol.
41
no.
1
pp.
1-8
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Genetic analysis of Xp22. 3 micro-deletions in seventeen families segregating isolated form of X-linked ichthyosis
Raja Hussain Ali, Sabba Mahmood, Syed Irfan Raza, Abdul Aziz, Syed Kamran-ul-Hassan Naqvi, Naveed Wasif, Muhammad Ansar, Wasim Ahmad, Sayed Hajan Shah, Bakht Tarin Khan, Qaiser Zaman, Ajab Gul, Abdul Wali, Ghazanfar Ali, Saadulah Khan, Muhammad Khisroon, Sulman Basit
(2015)
Journal of Dermatological Science
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80
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3
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214-217
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