Expanding the phenotype of CRB2 mutations - A new ciliopathy syndrome? von Jaron, R., Rosenfeld, N., Zahdeh, F., Carmi, S., Beni-Adani, L., Doviner, V., Picard, E., Segel, R., Zeligson, S., Carmel, L., Renbaum, P., Levy-Lahad, E.

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A Single Nucleotide Polymorphism in the RAD51 Gene Modifies Cancer Risk in BRCA2 but Not BRCA1 Carriers von Levy-Lahad, E., Lahad, A., Eisenberg, S., Dagan, E., Paperna, T., Kasinetz, L., Catane, R., Kaufman, B., Beller, U., Renbaum, P., Gershoni-Baruch, R.

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Ovarian reserve and PGD treatment outcome in women with myotonic dystrophy von Srebnik, N, Margalioth, E.J, Rabinowitz, R, Varshaver, I, Altarescu, G, Renbaum, P, Levi-Lahad, E, Weintraub, A, Eldar-Geva, T

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Familial haplotyping and embryo analysis for Preimplantation Genetic Diagnosis (PGD) using DNA microarrays: a proof of principle study von Altarescu, G., Zeevi, D. A., Zeligson, S., Perlberg, S., Eldar-Geva, T., Margalioth, E. J., Levy-Lahad, E., Renbaum, P.

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Single-sperm analysis for haplotype construction of de-novo paternal mutations: application to PGD for neurofibromatosis type 1 von Altarescu, G., Brooks, B., Kaplan, Y., Eldar-Geva, T., Margalioth, E.J., Levy-Lahad, E., Renbaum, P.

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P-2 Overcoming limitations of single cell analysis in duplicated and GC-rich genomic regions using multiple displacement amplification for preimplantation genetic diagnosis (PGD) von Zeevi, D.A, Renbaum, P, Eldar-Geva, T, Ron-El, R, Raziel, A, Brooks, B, Strassburger, D, Margalioth, E.J, Levy-Lahad, E, Altarescu, G

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O-22 Embryo biopsy for PGD has no significant impact on neonatal outcome von Eldar-Geva, T, Srebnik, N, Margalioth, E.J, Schonberger, O, Varshaver, I, Perez, A, Rubinstein, E, Renbaum, P, Dekel, N, Levy-Lahad, E, Altarescu, G

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P2 Instant familial haplotyping in conjunction with embryo analysis in preimplantation genetic diagnosis (PGD) using DNA microarrays von Altarescu, G, Zeevi, D.A, Zeligson, S, Perlberg, S, Geva, T. Eldar, Varshaver, I, Margalioth, E.J, Lahad, E.L, Renbaum, P

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O1 Preimplantation Genetic Diagnosis (PGD) for germline mosaicism von Altarescu, G, Eldar-Geva, T, Brooks, B, Margalioth, E.J, Levy-Lahad, E, Renbaum, P

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Gilbert's syndrome and hyperbilirubinaemia in ABO-incompatible neonates von Kaplan, Michael, Hammerman, Cathy, Renbaum, Paul, Klein, Gaya, Levy-Lahad, Ephrat

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Successful polar body-based preimplantation genetic diagnosis for achondroplasia von Altarescu, G, Renbaum, P, P, B Brooks, Margalioth, EJ, Chetrit, A Ben, Munter, G, Levy-Lahad, E, Eldar-Geva, T

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Advantages of multiple markers and polar body analysis in preimplantation genetic diagnosis for Alagille disease von Renbaum, P., Brooks, B., Kaplan, Y., Eldar-Geva, T., Margalioth, E J., Levy-Lahad, E., Altarescu, G.

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50. ASSESSMENT OF MICROBIAL CONTAMINATION TO ELIMINATE ARTIFACTS IN SEQUENCING-BASED PGT-A/PGT-SR von Altarescu, G., Granit, R., Dror, T., Kirshberg, S., Rosen, T., Shaviv, S., Zeligson, S., Beeri, R., Renbaum, P., Zeevi, D.A.

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O8 Preimplantation genetic diagnosis (PGD) for monogenic disorders. When blastomere analysis may be impossible von Renbaum, P, Eldar-Geva, T, Beeri, R, Varshower, I, Brooks, B, Zylber Haran, E, Margalioth, E.J, Levy-Lahad, E, Altarescu, G

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Monogenic determinants of familial Alzheimer's disease: presenilin-2 mutations von Renbaum, P, Levy-Lahad, E

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Polar Body-Based Preimplantation Genetic Diagnosis for N-Acetylglutamate Synthase Deficiency von Altarescu, G., Brooks, B., Eldar-Geva, T., Margalioth, E.J., Singer, A., Levy-Lahad, E., Renbaum, P.

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Differing pathogenesis of perinatal bilirubinemia in glucose-6-phosphate dehydrogenase-deficient versus -normal neonates von KAPLAN, Michael, HAMMERMAN, Cathy, RENBAUM, Paul, LEVY-LAHAD, Ephrat, VREMAN, Hendrik J, STEVENSON, David K

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Gilbert Syndrome and Glucose-6-Phosphate Dehydrogenase Deficiency: A Dose-Dependent Genetic Interaction Crucial to Neonatal Hyperbilirubinemia von Kaplan, M, Renbaum, P, Levy-Lahad, E, Hammerman, C, Lahad, A, Beutler, E

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PGD for fragile X syndrome: ovarian function is the main determinant of success von Tsafrir, Avi, Altarescu, Gheona, Margalioth, Ehud, Brooks, Baruch, Renbaum, Paul, Levy-Lahad, Ephrat, Rabinowitz, Ron, Varshaver, Irit, Eldar-Geva, Talia

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Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population von Shaag, Avraham, Walsh, Tom, Renbaum, Paul, Kirchhoff, Tomas, Nafa, Khedoudja, Shiovitz, Stacey, Mandell, Jessica B., Welcsh, Piri, Lee, Ming K., Ellis, Nathan, Offit, Kenneth, Levy-Lahad, Ephrat, King, Mary-Claire

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