Your search returned 9 results.

Results
	1.	A new case confirming and expanding the phenotype spectrum of ADAT3-related intellectual disability syndrome. [electronic resource] by Sharkia, Rajech Zalan, Abdelnaser Jabareen-Masri, Azhar Zahalka, Hazar Mahajnah, Muhammad Producer: 20200206 In: European journal of medical genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The changing pattern of consanguinity in a selected region of the Israeli Arab community. [electronic resource] by Sharkia, Rajach Zaid, Muhamad Athamna, Abed Cohen, Dani Azem, Abdussalam Zalan, Abdelnaser Producer: 20080129 In: American journal of human biology : the official journal of the Human Biology Council vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Exploration of Risk Factors for Type 2 Diabetes among Arabs in Israel. [electronic resource] by Sharkia, Rajech Sheikh-Muhammad, Ahmad Mahajnah, Muhammad Khatib, Mohammad Zalan, Abdelnaser Producer: 20200514 In: Annals of global health vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	CHANGES IN MARRIAGE PATTERNS AMONG THE ARAB COMMUNITY IN ISRAEL OVER A 60-YEAR PERIOD. [electronic resource] by Sharkia, Rajech Mahajnah, Muhammad Athamny, Esmael Khatib, Mohammad Sheikh-Muhammad, Ahmad Zalan, Abdelnaser Producer: 20170112 In: Journal of biosocial science vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Factors affecting the utilization of genetic counseling services among Israeli Arab women. [electronic resource] by Sharkia, Rajech Tarabeia, Jalal Zalan, Abdelnaser Atamany, Esmael Athamna, Muhammad Allon-Shalev, Stavit Producer: 20160301 In: Prenatal diagnosis vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Sanfilippo type A: new clinical manifestations and neuro-imaging findings in patients from the same family in Israel: a case report. [electronic resource] by Sharkia, Rajech Mahajnah, Muhammad Zalan, Abdelnaser Sourlis, Chrysovalantis Bauer, Peter Schöls, Ludger Producer: 20140306 In: Journal of medical case reports vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Comparative screening of FMF mutations in various communities of the Israeli society. [electronic resource] by Sharkia, Rajech Mahajnah, Muhammad Zalan, Abdelnaser Athamna, Muhammad Azem, Abdussalam Badarneh, Khader Faris, Fuad Producer: 20140128 In: European journal of medical genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A novel biallelic loss-of-function mutation in TMCO1 gene confirming and expanding the phenotype spectrum of cerebro-facio-thoracic dysplasia. [electronic resource] by Sharkia, Rajech Zalan, Abdelnaser Jabareen-Masri, Azhar Hengel, Holger Schöls, Ludger Kessel, Amit Azem, Abdussalam Mahajnah, Muhammad Producer: 20200708 In: American journal of medical genetics. Part A vol. 179 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Homozygous mutation in PTRH2 gene causes progressive sensorineural deafness and peripheral neuropathy. [electronic resource] by Sharkia, Rajech Shalev, Stavit A Zalan, Abdelnaser Marom-David, Milit Watemberg, Nathan Urquhart, Jill E Daly, Sarah B Bhaskar, Sanjeev S Williams, Simon G Newman, William G Spiegel, Ronen Azem, Abdussalam Elpeleg, Orly Mahajnah, Muhammad Producer: 20171030 In: American journal of medical genetics. Part A vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)