Whole-Exome Sequencing Identifies a Novel Homozygous Frameshift Mutation in the MTMR2 Gene as a Causative Mutation in a Patient with Charcot-Marie-Tooth Disease Type 4B1 von Abdalla-Moady, Tameemi, Peleg, Amir, Sadeh, Orit, Badarneh, Khader, Fares, Fuad

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Comparative screening of FMF mutations in various communities of the Israeli society von Sharkia, Rajech, Mahajnah, Muhammad, Zalan, Abdelnaser, Athamna, Muhammad, Azem, Abdussalam, Badarneh, Khader, Faris, Fuad

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Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated? von Fares, Fuad, Badarneh, Khader, Abosaleh, Mohamed, Harari-Shaham, Amalia, Diukman, Roni, David, Miriam

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The Effect of Gender and Arm Anatomical Position on the Hand Grip Strength and Fatigue Resistance during Sustained Maximal Handgrip Effort von Almashaqbeh, Sami Faris, Al-Momani, Sajidah, Khader, Ateka, Qananwah, Qasem, Marabeh, Saja, Maabreh, Rand, Al Badarneh, Ayat, Abdullah, Kawther

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