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Al‐Muhaizea, Mohammed A., Aldeeb, Hanouf, Almass, Rawan, Jaber, Hadeel, Binhumaid, Felwa, Alquait, Laila, Abukhalid, Musaad, Aldhalaan, Hesham, Alsagob, Maysoon, Al‐Bakheet, Albandary, Aldosary, Mazhor, Alkofide, Hadeel, Alrasheed, Maha M., Colak, Dilek, Kaya, Namik
Published in Annals of human genetics (01.01.2022)
Published in Annals of human genetics (01.01.2022)
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Patient demographics and characteristics from an ambispective, observational study of patients with duchenne muscular dystrophy in Saudi Arabia
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Published in Frontiers in pediatrics (30.09.2022)
Published in Frontiers in pediatrics (30.09.2022)
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Molecular and clinical spectra of FBXL4 deficiency
El‐Hattab, Ayman W., Dai, Hongzheng, Almannai, Mohammed, Wang, Julia, Faqeih, Eissa A., Al Asmari, Ali, Saleh, Mohammed A. M., Elamin, Mohammed A. O., Alfadhel, Majid, Alkuraya, Fowzan S., Hashem, Mais, Aldosary, Mazhor S., Almass, Rawan, Almutairi, Faten B., Alsagob, Maysoon, Al‐Owain, Mohammed, Al‐Sharfa, Shirin, Al‐Hassnan, Zuhair N., Rahbeeni, Zuhair, Al‐Muhaizea, Mohammed A., Makhseed, Nawal, Foskett, Gretchen K., Stevenson, David A., Gomez‐Ospina, Natalia, Lee, Chung, Boles, Richard G., Schrier Vergano, Samantha A., Wortmann, Saskia B., Sperl, Wolfgang, Opladen, Thomas, Hoffmann, Georg F., Hempel, Maja, Prokisch, Holger, Alhaddad, Bader, Mayr, Johannes A., Chan, Wenyaw, Kaya, Namik, Wong, Lee‐Jun C.
Published in Human mutation (01.12.2017)
Published in Human mutation (01.12.2017)
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