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Results: 1-8 |
Results: 8
Differences in rhythms of enzymatic activity of maternal and fetal blood
Authors: Peleg, L Wilf-Miron, R Goldman, B Ashkenazi, I
Citation: L. Peleg et al., Differences in rhythms of enzymatic activity of maternal and fetal blood, CHRONOBIO I, 17(2), 2000, pp. 221-228
Clinical manifestations of psychiatric patients who are carriers of Tay-Sachs disease - Possible role of psychotropic drugs
Authors: Zelnik, N Khazanov, V Sheinkman, A Karpati, AM Peleg, L
Citation: N. Zelnik et al., Clinical manifestations of psychiatric patients who are carriers of Tay-Sachs disease - Possible role of psychotropic drugs, NEUROPSYCHB, 41(3), 2000, pp. 127-131
Screening for fragile X syndrome in women of reproductive age
Authors: Pesso, R Berkenstadt, H Cuckle, H Gak, E Peleg, L Frydman, M Barkai, G
Citation: R. Pesso et al., Screening for fragile X syndrome in women of reproductive age, PRENAT DIAG, 20(8), 2000, pp. 611-614
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 techniques
Authors: Aviram-Goldring, A Goldman, B Netanelov-Shapira, I Chen-Shtoyerman, R Zvulunov, A Tal, O Ilan, T Peleg, L
Citation: A. Aviram-goldring et al., 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 techniques, INT J DERM, 39(3), 2000, pp. 182-187
A novel mutation in the HEXA gene specific to Tay-Sachs disease carriers of Jewish Iraqi origin
Authors: Karpati, M Peleg, L Gazit, E Akstein, E Goldman, B
Citation: M. Karpati et al., A novel mutation in the HEXA gene specific to Tay-Sachs disease carriers of Jewish Iraqi origin, CLIN GENET, 57(5), 2000, pp. 398-400
A novel allele in the promoter region of the human serotonin transporter gene
Authors: Michaelovsky, E Frisch, A Rockah, R Peleg, L Magal, N Shohat, M Weizman, R
Citation: E. Michaelovsky et al., A novel allele in the promoter region of the human serotonin transporter gene, MOL PSYCHI, 4(1), 1999, pp. 97-99
Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewishpopulation (vol 12, pg 240, 1998)
Authors: Horowitz, M Pasmanik-Chor, M Borochowitz, Z Falik-Zaccai, T Heldmann, K Carmi, R Parvari, R Beit-Or, H Goldman, B Peleg, L Levy-Lahad, E Renbaum, P Legum, S Shomrat, R Yeger, H Benbenisti, D Navon, R Dror, V Shohat, M Magal, N Navot, N Eyal, N
Citation: M. Horowitz et al., Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewishpopulation (vol 12, pg 240, 1998), HUM MUTAT, 13(3), 1999, pp. 255-255
Heat stable and urea resistant alkaline phosphatase in maternal neutrophils from normal and dawn syndrome pregnancies
Authors: Peleg, L Ries, L Getslev, V Lusky, A Chaki, R Lipitz, S Barkai, G
Citation: L. Peleg et al., Heat stable and urea resistant alkaline phosphatase in maternal neutrophils from normal and dawn syndrome pregnancies, PRENAT DIAG, 19(3), 1999, pp. 224-228
Risultati: 1-8 |