Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy von Desir, Julie, Moya, Graciela, Reish, Orit, Van Regemorter, Nicole, Deconinck, Hilde, David, Karen L, Meire, Françoise M, Abramowicz, Marc J

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Sporadic Aneuploidy in PHA-Stimulated Lymphocytes of Trisomies 21, 18, and 13 von Reish, O., Regev, M., Kanesky, A., Girafi, S., Mashevich, M.

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Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) gene von Fullston, T, Finnis, M, Hackett, A, Hodgson, B, Brueton, L, Baynam, G, Norman, A, Reish, O, Shoubridge, C, Gecz, J

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The increased expression of 14q32 small nucleolar RNA transcripts in promyelocytic leukemia cells is not dependent on PML–RARA fusion gene von Cohen, Y, Hertzog, K, Reish, O, Mashevich, M, Garach-Jehoshua, O, Bar-Chaim, A, Trakhtenbrot, L, Kornberg, A

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OP15.08: Fetal abnormalities leading to 3rd trimester abortion: 9 year experience from a single Medical Center von Barel, O., Vaknin, Z., Smorgick, N., Reish, O., Mendelovic, S., Herman, A., Maymon, R.

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Is there an increased rate of megacystis in twins? von Maymon, R., Ben‐Ami, I., Vaknin, Z., Reish, O., Herman, A.

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Brain anomalies associated with 47,XYY karyotypes detected on a prenatal scan von Maymon, R., Herman, A., Reish, O.

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Glu274Lys/Gly309Arg Mutation of the Tissue‐Nonspecific Alkaline Phosphatase Gene in Neonatal Hypophosphatasia Associated with Convulsions von Litmanovitz, I., Reish, O., Dolfin, T., Arnon, S., Regev, R., Grinshpan, G., Yamazaki, M., Ozono, K.

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An outbreak of multiresistant Klebsiella in a neonatal intensive care unit von Reish, O., Ashkenazi, S., Naor, N., Samra, Z., Merlob, P.

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Congenital Short-Bowel and Malrotation: Clinical Presentation and Outcome of Six Affected Offspring in Three Related Families von Erez, I., Reish, O., Kovalivker, M., Lazar, L., Raz, A., Katz, S.

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Prenatal diagnosis for detecting congenital malformations: acceptance among Israeli Arab women von Jaber, L, Dolfin, T, Shohat, T, Halpern, G J, Reish, O, Fejgin, M

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Replication status as a possible marker for genomic instability in cells originating from genotypes with balanced rearrangements von Amiel, A, Levi, E, Reish, O, Sharony, R, Fejgin, M D

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Replication asynchrony increases in women at risk for aneuploid offspring von Amiel, A, Reish, O, Gaber, E, Kedar, I, Diukman, R, Fejgin, M

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Frequencies of C282Y and H63D alleles in the HFE gene among various Jewish ethnic groups in Israel: A change of concept required von Reish, Orit, Shefer-Kaufmann, Niva, Shimshoni, Daphne Chapman, Renbaum, Paul, Orr-Urtreger, Avi, Steiner, Hillel, Rapoport, Micha, Levy-Lahad, Ephrat, Altarescu, Gheona

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OP15.08: Fetal abnormalities leading to 3 rd trimester abortion: 9 year experience from a single Medical Center von Barel, O., Vaknin, Z., Smorgick, N., Reish, O., Mendelovic, S., Herman, A., Maymon, R.

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Ranitidine-induced bradycardia in a neonate : a first report von NAHUM, E, REISH, O, NAOR, N, MERLOB, P

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ARE ALL PHENOTYPICALLY-NORMAL TURNER SYNDROME FETUSES MOSAICS? von AMIEL, A., KIDRON, D., KEDAR, I., GABER, E., REISH, O., FEJGIN, M. D.

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Dynamic modification strategy of the Israeli prenatal carrier screening protocol: inclusion of the oriental Jewish group to the cystic fibrosis panel—update von Reish, Orit, Shohat, Mordechai, Magal, Nurit, Pesso, Rachel, Borochowitz, Zvi U, Adir, Vardit, Karpati, Mazal, Shimshoni, Daphne Chapman

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Analysis of mesenchymal cells derived from an chondrodysplasia punctuate patient and donors von Shur, Irena, Reish, Orit, Ezra, Eli, Benayahu, Dafna

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Dynamic modification strategy of the Israeli carrier screening protocol: inclusion of the Oriental Jewish Group to the cystic fibrosis panel von Reish, Orit, Borochowitz, Zvi U., Adir, Vardit, Shohat, Mordechai, Karpati, Mazal, Shtorch, Atalia, Orr-Urtreger, Avi, Yaron, Yuval, Shalev, Stavit, Fares, Fuad, Gershoni-Baruch, Ruth, Falik-Zaccai, Tzipora C., Chapman-Shimshoni, Daphne

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