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Israel Journal of Medical Sciences|March 1, 1986
Improved reliability of a serum alpha-fetoprotein enzyme immunoassay compared with a radioimmunoassayL Peleg, H Slor, T Cordova, et al.
Annals of Human Biology|March 5, 2002
Protein electrophoretic markers in Israel: compilation of data and genetic affinitiesA Zoossmann-Diskin, A Joel, M Liron, et al.
Prenatal Diagnosis|August 22, 2000
Screening for fragile X syndrome in women of reproductive ageR Pesso, M Berkenstadt, H Cuckle, et al.
Prenatal Diagnosis|April 21, 1999
Heat stable and urea resistant alkaline phosphatase in maternal neutrophils from normal and Down syndrome pregnanciesL Peleg, L Ries, V Getslev, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Lower frequency of Gaucher disease carriers among Tay-Sachs disease carriersL Peleg, A Frisch, B Goldman, et al.
Molecular Psychiatry|March 24, 1999
A novel allele in the promoter region of the human serotonin transporter geneE Michaelovsky, A Frisch, R Rockah, et al.
Cancer Chemotherapy and Pharmacology|July 8, 1998
Time dependency of hematopoietic growth factor coupled to chronotoxicity of carboplatinI G Ron, L Peleg, S Rienstein, et al.
Human Mutation|January 1, 1997
Tay-Sachs disease and HEXA mutations among Moroccan JewsM Kaufman, J Grinshpun-Cohen, M Karpati, et al.
International Journal of Dermatology|April 12, 2000
Deletion patterns of the STS gene and flanking sequences in Israeli X-linked ichthyosis patients and carriers: analysis by polymerase chain reaction and fluorescence in situ hybridization techniquesA Aviram-Goldring, B Goldman, I Netanelov-Shapira, et al.
Human Mutation|September 23, 1998
Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewish populationM Horowitz, M Pasmanik-Chor, Z Borochowitz, et al.
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