A Voice from within: A Challenge for the Conservative Jewish Movement and Its Gay/Lesbian Activists von Krawitz, Cole

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BEYOND BIG BUCKS AND MEDIA SAVVY von Cole Krawitz

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Beyond big bucks and media savvy: an interview with Jean Hardisty and Esther Kaplan on the rise of the conservative movement in the U.S. and Jewish social justice work today von Krawitz, Cole

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TENSE DIALOGUES: SPEAKING (ACROSS) MULTICULTURAL DIFFERENCES IN THE JEWISH FEMINIST WORLD: A VOICE FROM WITHIN: A CHALLENGE FOR THE CONSERVATIVE JEWISH MOVEMENT AND ITS GAY/LESBIAN... von Krawitz, Cole

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A Voice from Within: A Challenge for the Conservative Jewish Movement and its Gay/Lesbian Activists von Krawitz, Cole

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Beyond Big Bucks and Media Savvy: An Interview with Jean Hardisty and Esther Kaplan on the Rise of the Conservative Movement in the U.S. and Jewish Social Justice Work Today von Krawitz, Cole, Hardisty, Jean V, Kaplan, Esther

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Beyond Big Bucks and Media Savvy: An Interview with Jean Hardisty and Esther Kaplan on the Rise of the Conservative Movement in the U. S. and Jewish Social Justice Work Today von Kaplan, Esther, Hardisty, Jean, Krawitz, Cole

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Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome von Mundlos, Stefan, Robinson, Peter N, Krawitz, Peter M, Schweiger, Michal R, Rödelsperger, Christian, Marcelis, Carlo, Kölsch, Uwe, Meisel, Christian, Stephani, Friederike, Kinoshita, Taroh, Murakami, Yoshiko, Bauer, Sebastian, Isau, Melanie, Fischer, Axel, Dahl, Andreas, Kerick, Martin, Hecht, Jochen, Köhler, Sebastian, Jäger, Marten, Grünhagen, Johannes, de Condor, Birgit Jonske, Doelken, Sandra, Brunner, Han G, Meinecke, Peter, Passarge, Eberhard, Thompson, Miles D, Cole, David E, Horn, Denise, Roscioli, Tony

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A post glycosylphosphatidylinositol (GPI) attachment to proteins, type 2 (PGAP2) variant identified in Mabry syndrome index cases: Molecular genetics of the prototypical inherited... von Thompson, Miles D., Knaus, Alexej A., Barshop, Bruce A., Caliebe, Almuth, Muhle, Hiltrud, Nguyen, Thi Tuyet Mai, Baratang, Nissan V., Kinoshita, Taroh, Percy, Maire E., Campeau, Philippe M., Murakami, Yoshiko, Cole, David E., Krawitz, Peter M., Mabry, C. Charlton

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Rare Noncoding Mutations Extend the Mutational Spectrum in the PGAP3 Subtype of Hyperphosphatasia with Mental Retardation Syndrome von Knaus, Alexej, Awaya, Tomonari, Helbig, Ingo, Afawi, Zaid, Pendziwiat, Manuela, Abu-Rachma, Jubran, Thompson, Miles D., Cole, David E., Skinner, Steve, Annese, Fran, Canham, Natalie, Schweiger, Michal R., Robinson, Peter N., Mundlos, Stefan, Kinoshita, Taroh, Munnich, Arnold, Murakami, Yoshiko, Horn, Denise, Krawitz, Peter M.

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Biallelic variants in PIGN cause Fryns syndrome, multiple congenital anomalies-hypotonia-seizures syndrome, and neurologic phenotypes: A genotype–phenotype correlation study von Loong, Lucy, Tardivo, Agostina, Knaus, Alexej, Hashim, Mona, Pagnamenta, Alistair T., Alt, Kerstin, Böhrer-Rabel, Helena, Caro-Llopis, Alfonso, Cole, Trevor, Distelmaier, Felix, Edery, Patrick, Ferreira, Carlos R., Jezela-Stanek, Aleksandra, Kerr, Bronwyn, Kluger, Gerhard, Krawitz, Peter M., Kuhn, Marius, Lemke, Johannes R., Lesca, Gaetan, Lynch, Sally Ann, Martinez, Francisco, Maxton, Caroline, Mierzewska, Hanna, Monfort, Sandra, Nicolai, Joost, Orellana, Carmen, Pal, Deb K., Płoski, Rafał, Quarrell, Oliver W., Rosello, Monica, Rydzanicz, Małgorzata, Sabir, Ataf, Śmigiel, Robert, Stegmann, Alexander P.A., Stewart, Helen, Stumpel, Constance, Szczepanik, Elżbieta, Tzschach, Andreas, Wolfe, Lynne, Taylor, Jenny C., Murakami, Yoshiko, Kinoshita, Taroh, Bayat, Allan, Kini, Usha

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Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome) von Thompson, Miles D., Roscioli, Tony, Marcelis, Carlo, Nezarati, Marjan M., Stolte-Dijkstra, Irene, Sharom, Frances J., Lu, Peihua, Phillips, John A., Sweeney, Elizabeth, Robinson, Peter N., Krawitz, Peter, Yntema, Helger G., Andrade, Danielle M., Brunner, Han G., Cole, David E.C.

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Rare Noncoding Mutations Extend the Mutational Spectrum in the PGAP3 Subtype of Hyperphosphatasia with Mental Retardation Syndrome von Knaus, A, Awaya, T, Helbig, I, Afawi, Z, Pendziwiat, M, Abu-Rachma, J, Thompson, MD, Cole, DE, Skinner, S, Annese, F, Canham, N, Schweiger, MR, Robinson, PN, Mundlos, S, Kinoshita, T, Munnich, A, Murakami, Y, Horn, D, Krawitz, PM

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