Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield
Anazi, S, Maddirevula, S, Faqeih, E, Alsedairy, H, Alzahrani, F, Shamseldin, H E, Patel, N, Hashem, M, Ibrahim, N, Abdulwahab, F, Ewida, N, Alsaif, H S, Al Sharif, H, Alamoudi, W, Kentab, A, Bashiri, F A, Alnaser, M, AlWadei, A H, Alfadhel, M, Eyaid, W, Hashem, A, Al Asmari, A, Saleh, M M, AlSaman, A, Alhasan, K A, Alsughayir, M, Al Shammari, M, Mahmoud, A, Al-Hassnan, Z N, Al-Husain, M, Osama Khalil, R, Abd El Meguid, N, Masri, A, Ali, R, Ben-Omran, T, El Fishway, P, Hashish, A, Ercan Sencicek, A, State, M, Alazami, A M, Salih, M A, Altassan, N, Arold, S T, Abouelhoda, M, Wakil, S M, Monies, D, Shaheen, R, Alkuraya, F S
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Published in Molecular psychiatry (01.04.2017)
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Epileptic encephalopathy with continuous spike-and-wave during sleep maps to a homozygous truncating mutation in AMPA receptor component FRRS1L: Letter to the Editor
Shaheen, R., Al Tala, S., Ewida, N., Abouelhoda, M., Alkuraya, F.S.
Published in Clinical genetics (01.09.2016)
Published in Clinical genetics (01.09.2016)
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