Harel-Yoon syndrome: the first case report from Saudi Arabia by Alaa AlAyed, Manar A. Samman, Abdul Ali Peer-Zada, Mohammed Almannai

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Favorable outcome of PML‐RARα short isoform and FLT3‐ITD mutation in a patient with several adverse prognostic markers: A case report by Mohammed A. Bafail, Rahaf AlTahan, Manar A. Samman, Suha A. Tashkandi, Ibraheem H. Motabi, Abdul Ali Peer‐Zada

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Fatal intracranial haemorrhage in acute promyelocytic leukemia patients with short isoform of PML-RARα: Review of molecular and radiological data by Manal Abudawood, Hanan Alorini, Manar A. Samman, Salman M. Bashir, Azizah AlSwayed, Sarah Binhassan, Abdul Ali Peer-Zada

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Neurological and extra-neurological clinical spectrum observed in pediatric patients with EMC1 gene variants identified by whole exome sequencing by Abdul Ali Peer-Zada, Osama A. Obaid, Manar A. Samman, Aqeela AlHashim, Hajar AlAsmari, Ali M. AlAsmari

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Reclassifying variations of unknown significance in diseases affecting Saudi Arabia’s population reveal new associations by Mariam M. Al Eissa, Mariam M. Al Eissa, Raniah S. Alotibi, Raniah S. Alotibi, Bader Alhaddad, Bader Alhaddad, Taghrid Aloraini, Taghrid Aloraini, Manar S. Samman, Abdulrahman AlAsiri, Abdulrahman AlAsiri, Mohamed Abouelhoda, Amerh S. AlQahtani

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A GRM7 mutation associated with developmental delay reduces mGlu7 expression and produces neurological phenotypes by Nicole M. Fisher, Aqeela AlHashim, Aditi B. Buch, Hana Badivuku, Manar M. Samman, Kelly M. Weiss, Gabriela I. Cestero, Mark D. Does, Jerri M. Rook, Craig W. Lindsley, P. Jeffrey Conn, Rocco G. Gogliotti, Colleen M. Niswender

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