Epidermal mosaicism and Blaschko's lines von Chemke, J

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Genetic Services in Israel von Chemke, J., Zlotogora, J.

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Pelvis-shoulder dysplasia von HAUSER, S. E, CHEMKE, J. M, BANKIER, A

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Medical genetics in Israel von Zlotogora, J, Chemke, J

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Autosomal recessive inheritance of Nager acrofacial dysostosis von Chemke, J, Mogilner, B M, Ben-Itzhak, I, Zurkowski, L, Ophir, D

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CYTOGENETIC ANALYSIS OF FETAL CHONDROCYTES: A COMPARATIVE STUDY von GELMAN-KOHAN, Z., ROSENSAFT, J., BEN-HUR, H., HABER, A., CHEMKE, J.

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Teratogenicity of Progestogens Given During the First Trimester of Pregnancy von KATZ, Z, LANCET, M, SKORNIK, J, CHEMKE, J, MOGILNER, B M, KLINBERG, M

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Aberrant melanoblast migration associated with trisomy 18 mosaicism von Chemke, J, Rappaport, S, Etrog, R

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COL11A2 mutation associated with autosomal recessive Weissenbacher-Zweymuller syndrome: Molecular and clinical overlap with otospondylomegaepiphyseal dysplasia (OSMED) von Harel, Tamar, Rabinowitz, Ronen, Hendler, Netta, Galil, Aharon, Flusser, Hagit, Chemke, Juan, Gradstein, Libe, Lifshitz, Tova, Ofir, Rivka, Elbedour, Khalil, Birk, Ohad S.

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Further delineation of the acrocallosal syndrome von Gelman-Kohan, Z, Antonelli, J, Ankori-Cohen, H, Adar, H, Chemke, J

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Homozygosity for inversion (2)(q12q14) von GELMAN-KOHAN, Z, ROSENSAFT, J, NISANI BEN-COHEN, R, CHEMKE, J

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3‐Methylglutaconic aciduria: A marker for as yet unspecified disorders and the relevance of prenatal diagnosis in a ‘new’ type (‘type 4’) von Chitayat, D., Chemke, J., Gibson, K. M., Mamer, O. A., Kronick, J. B., McGill, J. J., Rosenblatt, B., Sweetman, L., Scriver, C. R.

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Isolated foveal hypoplasia von Oliver, M D, Dotan, S A, Chemke, J, Abraham, F A

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Chorionic villus sampling for fetal karyotyping in missed abortions von Appleman, Z., Rosensaft, J., Elchalal, U., Caspi, B., Chemke, J.

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Familial café au lait spots: a variant of neurofibromatosis type 1 von Abeliovich, D, Gelman-Kohan, Z, Silverstein, S, Lerer, I, Chemke, J, Merin, S, Zlotogora, J

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The dilemma of chromosomal mosaicism in chorionic villus sampling-'direct' versus long-term cultures von Nisani, R., Chemke, J., Voss, R., Appelman, Z., Caspi, B., Lewin, A., Dar, H., Reiter, A.

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Weissenbacher-Zweymüller syndrome: A distinct autosomal recessive skeletal dysplasia von Chemke, Juan, Carmi, Rivka, Galil, Aharon, Bar-Ziv, Yaakov, Ben-Ytzhak, Ilan, Zurkowski, Loretta

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Trisomy 9 confined to the placenta: Prenatal diagnosis and neonatal follow-up von Appelman, Z., Rosensaft, J., Chemke, J., Caspi, B., Ashkenazi, M., Mogilner, M. B.

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Homozygosity for autosomal dominant Marfan syndrome von Chemke, J, Nisani, R, Feigl, A, Garty, R, Cooper, M, Bårash, Y, Duksin, D

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Familial Recurring Thanatophoric Dwarfism: A Case Report von GRAFF, G., CHEMKE, J., LANCET, M.

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