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	1.	Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families. [electronic resource] by Issa, Yasmin A Kamal, Lara Rayyan, Amal Abu Dweik, Dima Pierce, Sarah Lee, Ming K King, Mary-Claire Walsh, Tom Kanaan, Moien Producer: 20170616 In: European journal of human genetics : EJHG vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families. [electronic resource] by Shahin, Hashem Walsh, Tom Rayyan, Amal Abu Lee, Ming K Higgins, Jake Dickel, Diane Lewis, Kristen Thompson, James Baker, Carl Nord, Alex S Stray, Sunday Gurwitz, David Avraham, Karen B King, Mary-Claire Kanaan, Moien Producer: 20100629 In: European journal of human genetics : EJHG vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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