Chromosomal aberrations and gene expression profiles in non-small cell lung cancer von Dehan, E, Ben-Dor, A, Liao, W, Lipson, D, Frimer, H, Rienstein, S, Simansky, D, Krupsky, M, Yaron, P, Friedman, E, Rechavi, G, Perlman, M, Aviram-Goldring, A, Izraeli, S, Bittner, M, Yakhini, Z, Kaminski, N

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Chromosomal microarray analysis of miscarriage products in recurrent pregnancy loss von Bar-Avin Dayan, D, Rienstein, S, Yonath, H, Guetta, E, Pras, E, Carp, H, Seidman, D

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P41 Chromosomal instability at different developmental stages of human preimplantation embryos von Dekel-Naftali, M, Aviram-Goldring, A, Litmanovitch, T, Shamash, J, Hourvitz, A, Yung, Y, Brengauz, M, Schiff, E, Rienstein, S

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Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia von Bar-joseph, Ifat, Pras, Elon, Reznik-Wolf, Haike, Marek-Yagel, Dina, Abu-Horvitz, Almogit, Dushnitzky, Maya, Goldstein, Nurit, Rienstein, Shlomit, Dekel, Michal, Pode-Shakked, Ben, Zlotnik, Joseph, Benarrosh, Anelia, Gillery, Philippe, Hofliger, Niklaus, Auray-Blais, Christiane, Garnotel, Roselyne, Anikster, Yair

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Proximal 19q Trisomy: A New Syndrome of Morbid Obesity and Mental Retardation von Zung, Amnon, Rienstein, Shlomit, Rosensaft, Jenny, Aviram-Goldring, Ayala, Zadik, Zvi

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Familial vs sporadic ovarian tumors: characteristic genomic alterations analyzed by CGH von Israeli, Ofir, Gotlieb, Walter H, Friedman, Eitan, Goldman, Boleslaw, Ben-Baruch, Gilad, Aviram-Goldring, Ayala, Rienstein, Shlomit

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P▪46 PGD for reciprocal and Robertsonian translocations: efficacy and limitations von Levron, J, Rienstein, S, Litmanovitch, T, Shamash, J, Barkai, G, Bider, D, Mashiach, S, Dor, J, Aviram-Goldring, A

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True hermaphroditism with ambiguous genitalia due to a complicated mosaic karyotype: Clinical features, cytogenetic findings, and literature review von Modan-Moses, Dalit, Litmanovitch, Talia, Rienstein, Shlomit, Meyerovitch, Joseph, Goldman, Boleslaw, Aviram-Goldring, Ayala

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P▪37 PGD for DiGeorge/velocardiofacial syndrome von Aviram-Goldring, A, Rienstein, S, Litmanovitz, T, Zalel, Y, Frydman, M, Gothielf, D, Barkai, G, Mashiach, S, Dor, J, Levron, J

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Comparative genomic hybridization analysis of radiation-associated and sporadic meningiomas von Rienstein, Shlomit, Loven, David, Israeli, Ofir, Ram, Zvi, Rappaport, Zvi Harry, Barkai, Gad, Goldman, Boleslaw, Aviram-Goldring, Ayala, Friedman, Eitan

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Daily Rhythms in Male Mice Meiosis von Rienstein, Shlomit, Dotan, Aviva, Avivi, Lydia, Ashkenazi, Israel

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Time dependency of hematopoietic growth factor coupled to chronotoxicity of carboplatin von RON, I. G, PELEG, L, RIENSTEIN, S, DOTAN, A, TICHER, A, WOLFSON, S, ASHKENAZI, I. E

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In silico chromosomal clustering of genes displaying altered expression patterns in ovarian cancer von Israeli, Ofir, Goldring-Aviram, Ayala, Rienstein, Shlomit, Ben-Baruch, Gilad, Korach, Jakob, Goldman, Boleslaow, Friedman, Eitan

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Genomic analyses of primary and metastatic serous epithelial ovarian cancer von Israeli, Ofir, Gotlieb, Walter H., Friedman, Eitan, Korach, Jacob, Friedman, Eddy, Goldman, Boleslaw, Zeltser, Assaf, Ben-Baruch, Gilad, Rienstein, Shlomit, Aviram-Goldring, Ayala

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Caudal dysplasia sequence with penile enlargement: Case report and a potential pathogenic hypothesis von Makhoul, Imad R., Aviram-Goldring, Ayala, Paperna, Tamar, Sujov, Polo, Rienstein, Shlomit, Smolkin, Tatiana, Epelman, Monica, Gershoni-Baruch, Ruth

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Do human embryos have the ability of self-correction? von Orvieto, Raoul, Shimon, Chen, Rienstein, Shlomit, Jonish-Grossman, Anat, Shani, Hagit, Aizer, Adva

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Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophrenia von Alkelai, Anna, Shohat, Shahar, Greenbaum, Lior, Schechter, Tanya, Draiman, Benjamin, Chitrit-Raveh, Eti, Rienstein, Shlomit, Dagaonkar, Neha, Hughes, Daniel, Aggarwal, Vimla S, Heinzen, Erin L, Shifman, Sagiv, Goldstein, David B, Kohn, Yoav

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Abnormal nuchal translucency followed by normal microarray analysis is associated with placental pathology‐related complications von Krispin, Eyal, Kushnir, Anya, Shemer, Asaf, Rienstein, Shlomit, Berkenstadt, Michal, Yinon, Yoav, Weisz, Boaz

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104: The association of pathological nuchal translucency to placental complications in cases of normal microarray analysis von Krispin, Eyal, Kushnir, Anya, Shemer, Assaf, Rienstein, Shlomit, Michal berekendt, Yinon, Yoav, Weisz, Boaz

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What have we learned from 691 prenatal chromosomal microarrays for ventricular septal defects? von Maya, Idit, Singer, Amihood, Yonath, Hagith, Reches, Adi, Rienstein, Shlomit, Zeligson, Sharon, Ben Shachar, Shay, Sagi‐Dain, Lena

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