Výsledky vyhledávání - Sher, Alam
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Novel splicing‐site mutation in DCAF17 gene causing Woodhouse‐Sakati syndrome in a large consanguineous family Autor Fozia, Fozia, Shah, Khadim, Nazli, Rubina, Khan, Sher Alam, Ahmad, Ijaz, Mohammad, Noor, Khan, Saadullah, Alotaibi, Amal
Vydáno 2021Text -
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A novel mutation in homeobox DNA binding domain of HOXC13 gene underlies pure hair and nail ectodermal dysplasia (ECTD9) in a Pakistani family Autor Khan, Anwar Kamal, Muhammad, Noor, Aziz, Abdul, Khan, Sher Alam, Shah, Khadim, Nasir, Abdul, Khan, Muzammil Ahmad, Khan, Saadullah
Vydáno 2017Text -
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Whole Exome Sequencing Confirms Molecular Diagnostics of Three Pakhtun Families With Autosomal Recessive Epidermolysis Bullosa Autor Fozia, Fozia, Nazli, Rubina, Bibi, Nousheen, Khan, Sher Alam, Muhammad, Noor, Shakeeb, Nafila, Khan, Saadullah, Jelani, Musharraf, Wasif, Naveed
Vydáno 2021Text -
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The Growth, physiological and biochemical response of foxtail millet to atrazine herbicide Autor Sher, Alam, Mudassir Maqbool, Muhammad, Iqbal, Javed, Nadeem, Muhammad, Faiz, Sajid, Noor, Hafeez, Hamid, Yasir, Yuan, Xiangyang, pingyi, Guo
Vydáno 2021Text -
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A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family Autor Khan, Sher Alam, Khan, Muhammad Adnan, Muhammad, Nazif, Bashir, Hina, Khan, Niamat, Muhammad, Noor, Yilmaz, Rüstem, Khan, Saadullah, Wasif, Naveed
Vydáno 2020Text -
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The First Report of a Missense Variant in RFX2 Causing Non-Syndromic Tooth Agenesis in a Consanguineous Pakistani Family Autor Khan, Sher Alam, Khan, Saadullah, Muhammad, Noor, Rehman, Zia Ur, Khan, Muhammad Adnan, Nasir, Abdul, Kalsoom, Umm-e-, Khan, Anwar Kamal, Khan, Hassan, Wasif, Naveed
Vydáno 2022Text -
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Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous families Autor Ullah, Asmat, Umair, Muhammad, Yousaf, Maryam, Khan, Sher Alam, Nazim-ud-din, Muhammad, Shah, Khadim, Ahmad, Farooq, Azeem, Zahid, Ali, Ghazanfar, Alhaddad, Bader, Rafique, Afzal, Jan, Abid, Haack, Tobias B., Strom, Tim M., Meitinger, Thomas, Ghous, Tahseen, Ahmad, Wasim
Vydáno 2017Text -
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Deleterious Variants in WNT10A, EDAR, and EDA Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations Autor Parveen, Asia, Khan, Sher Alam, Mirza, Muhammad Usman, Bashir, Hina, Arshad, Fatima, Iqbal, Maria, Ahmad, Waseem, Wahab, Ahsan, Fiaz, Amal, Naz, Sidra, Ashraf, Fareeha, Mobeen, Tayyaba, Aziz, Salman, Ahmed, Syed Shoaib, Muhammad, Noor, Hassib, Nehal F., Mostafa, Mostafa I., Gaboon, Nagwa E., Gul, Roquyya, Khan, Saadullah, Froeyen, Matheus, Shoaib, Muhammad, Wasif, Naveed
Vydáno 2019Text