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Browsing Universitätsbibliographie by Author "Khan, Amjad"

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Exome sequencing identifies homozygous variants in MBOAT7 associated with neurodevelopmental disorder

Nazmina, Gul; Khan, Amjad; Jiang, Jiuhong; Miao, Zhichao; Khan, Shahid Niaz; Khan, Muhammad Ismail; Shah, Abdul Haleem; Shah, Aysha Haleem; Khisroon, Muhammad; Haack, Tobias B. (2024)
Panoramic variation analysis of a family with neurodevelopmental disorders caused by biallelic loss-of-function variants in TMEM141, DDHD2, and LHFPL5

Sun, Liwei; Yang, Xueting; Khan, Amjad; Yu, Xue; Zhang, Han; Han, Shirui; Habulieti, Xiaerbati; Sun, Yang; Wang, Rongrong; Zhang, Xue (2024)
Variants of NAV3, a neuronal morphogenesis protein, cause intellectual disability, developmental delay, and microcephaly

Ghaffar, Amama; Akhter, Tehmeena; Stromme, Petter; Misceo, Doriana; Khan, Amjad; Frengen, Eirik; Umair, Muhammad; Isidor, Bertrand; Cogne, Benjamin; Khan, Asma A.; Bruel, Ange-Line; Sorlin, Arthur; Kuentz, Paul; Chiaverini, Christine; Innes, A. Micheil; Zech, Michael; Balaz, Marek; Havrankova, Petra; Jech, Robert; Ahmed, Zubair M.; Riazuddin, Sheikh; Riazuddin, Saima (2024)

Now showing items 1-3 of 3

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