A mutation in the saposin A coding region of the prosaposin gene in an infant presenting as Krabbe disease: first report of saposin A deficiency in humans von Spiegel, Ronen, Bach, Gideon, Sury, Vivi, Mengistu, Getu, Meidan, Bela, Shalev, Stavit, Yona Shneor, Mandel, Hanna, Zeigler, Marsha

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Prenatal diagnosis of 5p deletion syndrome following abnormally low maternal serum human chorionic gonadotrophin von Weiss, Amir, Shalev, Stavit, Weiner, Ehud, Shneor, Yona, Shalev, Eliezer

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Diversity of β-globin mutations in Israeli ethnic groups reflects recent historic events von FILON, D, ORON, V, ABRAMOV, A, RACHMILEWITZ, E. A, RUND, D, KAZAZIAN, H. H, OPPENHEIM, A, KRICHEVSKI, S, SHAAG, A, SHAAG, Y, WARREN, T. C, GOLDFARB, A, SHNEOR, Y, KOREN, A, AKER, M

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A frameshift mutation in codon 10 of the β-globin gene von Filon, Dvora, Oron, Varda, Shneor, Yona, Rund, Deborah, Oppenheim, Ariella

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