Skoura - a genetic island for congenital insensitivity to pain and anhidrosis among Moroccan Jews, as determined by a novel mutation in the NTRK1 gene von Suriu, C, Khayat, M, Weiler, M, Kfir, N, Cohen, C, Zinger, A, Aslanidis, C, Schmitz, G, Falik-Zaccai, TC

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Familial juvenile hypertrophy of the breast von Govrin-Yehudain, Jacky, Kogan, Leonid, Cohen, Hector.I., Falik-Zaccai, Tzipora C.

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A New Genetic Isolate of Gray Platelet Syndrome (GPS): Clinical, Cellular, and Hematologic Characteristics von Falik-Zaccai, Tzipora C, Anikster, Yair, Rivera, Candido E, Horne, McDonald K, Schliamser, Liliana, Phornphutkul, Chanika, Attias, Dina, Hyman, Tehila, White, James G, Gahl, William A

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Use of a cDNA microarray to determine molecular mechanisms involved in grey platelet syndrome von Hyman, Tehila, Huizing, Marjan, Blumberg, Peter M., Falik‐Zaccai, Tzipora C., Anikster, Yair, Gahl, William A.

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Mucolipidosis III type C: first-trimester biochemical and molecular prenatal diagnosis von Falik-Zaccai, T. C., Zeigler, M., Bargal, R., Bach, G., Borochowitz, Z., Raas-Rothschild, A.

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Coronary Heart Disease among Circassians in Israel Is Not Associated with Mutations in Thrombophilia Genes von FALIK-ZACCAI, TZIPORA C., HARON, YAFA, EILAT, DANNY, HARASH, BAKKY, GOLINKER, EKATERINA, HUSSEIN, OSAMAH, EISIKOVITS, RIVKA, BOROCHOWITZ, ZVI, LINN, SHAI

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Achondroplasia in diverse Jewish and Arab populations in Israel: clinical and molecular characterization von Falik-Zaccai, T C, Shachak, E, Abeliovitch, D, Lerer, I, Shefer, R, Carmi, R, Ries, L, Friedman, M, Shohat, M, Borochowitz, Z

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Phospholipase A2-activating protein is associated with a novel form of leukoencephalopathy von Falik Zaccai, TC, Savitzki, D, Zivony-Elboum, Y, Vilboux, T, Fitts, EC, Shoval, Y, Kalfon, L, Samra, N, Keren, Z, Gross, B, Chasnyk, N, Straussberg, R, Mullikin, JC, Teer, JK, Geiger, D, Kornitzer, D, Bitterman-Deutsch, O, Samson, AO, Wakamiya, M, Peterson, JW, Kirtley, ML, Pinchuk, IV, Baze, WB, Gahl, WA, Kleta, R, Anikster, Y, Chopra, AK

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Predisposition to the fragile X syndrome in jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype von FALIK-ZACCAI, T. C, SHACHAK, E, YALON, M, LIS, Z, BOROCHOWITZ, Z, MACPHERSON, J. N, NELSON, D. L, EICHLER, E. E

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