検索結果 - Sher, Alam
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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 著者: Khan, Anwar Kamal, Muhammad, Noor, Aziz, Abdul, Khan, Sher Alam, Shah, Khadim, Nasir, Abdul, Khan, Muzammil Ahmad, Khan, Saadullah
出版事項 2017テキスト -
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Whole Exome Sequencing Confirms Molecular Diagnostics of Three Pakhtun Families With Autosomal Recessive Epidermolysis Bullosa 著者: Fozia, Fozia, Nazli, Rubina, Bibi, Nousheen, Khan, Sher Alam, Muhammad, Noor, Shakeeb, Nafila, Khan, Saadullah, Jelani, Musharraf, Wasif, Naveed
出版事項 2021テキスト -
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The First Report of a Missense Variant in RFX2 Causing Non-Syndromic Tooth Agenesis in a Consanguineous Pakistani Family 著者: 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
出版事項 2022テキスト -
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Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous families 著者: 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
出版事項 2017テキスト -
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Deleterious Variants in WNT10A, EDAR, and EDA Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations 著者: 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
出版事項 2019テキスト