Deletion of the ANKRD15 gene at 9p24.3 causes parent-of-origin-dependent inheritance of familial cerebral palsy von Lerer, Israela, Sagi, Michal, Meiner, Vardiella, Cohen, Tirza, Zlotogora, Joel, Abeliovich, Dvorah

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Human heme oxygenase cDNA and induction of its mRNA by hemin von YOSHIDA, Tadashi, BIRO, Peter, COHEN, Tirza, MÜLLER, Rita M., SHIBAHARA, Shigeki

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Consanguinity in a population sample of Israeli Muslim Arabs, Christian Arabs and Druze von Vardi-Saliternik, R., Friedlander, Y., Cohen, T.

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Nucleotide sequence of the cDNA encoding human tyrosinase-related protein von COHEN, T, MULLER, R. M, TOMITA, Y, SHIBAHARA, S

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Sensorineural hearing loss in Jewish children born in Jerusalem von Levi, Haya, Tell, Lilly, Cohen, Tirza

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Molecular Basis for the Heterogeneity of Human Tyrosinase von SHIBAHARA, SHIGEKI, TOMITA, YASUSHI, TAGAMI, HACHIRO, MÜLLER, RITA M., COHEN, TIRZA

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Screening for five mutations detects 97% of cystic fibrosis (CF) chromosomes and predicts a carrier frequency of 1:29 in the Jewish Ashkenazi population von ABELIOVICH, D, LAVON, I. P, LERER, I, COHEN, T, SPRINGER, C, AVITAL, A, CUTTING, G. R

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Diaphragmatic defects in children of consanguineous parents von Arad, I, Lijovetzky, G C, Starinsky, R, Laufer, N, Cohen, T

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Mutations in PAX3 associated with waardenburg syndrome type I von Baldwin, Clinton T., Lipsky, Nina R., Hoth, Christopher F., Cohen, Tirza, Mamuya, Wilfred, Milunsky, Aubrey

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Evolution of a Genetic Disease in an Ethnic Isolate: β-Thalassemia in the Jews of Kurdistan von Rund, Deborah, Cohen, Tirza, Filon, Dvora, Dowling, Carol E., Warren, Tina C., Barak, Igal, Rachmilewitz, Eliezer, Kazazian, Haig H., Oppenheim, Ariella

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Structural organization of the pigment cell-specific gene located at the brown locus in mouse : its promoter activity and alternatively spliced transcripts von SHIBAHARA, S, TAGUCHI, H, MULLER, R. M, SHIBATA, K, COHEN, T, TOMITA, Y, TAGAMI, H

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A syndrome including thumb malformations, microcephaly, short stature, and hypogonadism von Zlotogora, J, Dagan, J, Ganen, A, Abu-Libdeh, M, Ben-Neriah, Z, Cohen, T

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The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22–q23 von Ziv, Yael, Rotman, Galit, Frydman, Moshe, Dagan, Judith, Cohen, Tirza, Foroud, Tatiana, Gatti, Richard A., Shiloh, Yosef

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Syndrome of brittle cornea, blue sclera, and joint hyperextensibility von Zlotogora, Joel, BenEzra, David, Cohen, Tirza, Cohen, Evelyne

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Familial hereditary thrombocytopenia and HLA von Naparstek, Yaakov, Abrahamov, Ayala, Cohen, Tirza, Brautbar, Chaim

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High frequency of congenital adrenal hyperplasia (classic 11β-hydroxylase deficiency) among Jews from Morocco von Rösler, Ariel, Leiberman, Esther, Cohen, Tirza

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Hypodontia: A Polygenic Trait-A Family Study among Israeli Jews von Chosack, Aubrey, Eidelman, Eliecer, Cohen, Tirza

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ALPHA-FETOPROTEIN DURING MID-TRIMESTER INDUCED ABORTION von Beyth, Yoram, Ron, Moshe, Alon, Jacob, Cohen, Tirza

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HLA-linked immune responsiveness to (T,G)-A-L: A family study von Suez, Daniel, Katz, Dvora, Brautbar, Chaim, Cohen, Tirza, Weisman, Ziva, Bentwich, Zvi, Mozes, Edna

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Genetic control of HLA-linked immune responsiveness to (H,G)-AL von Katz, Dvora, Suez, Daniel, Brautbar, Chaim, Cohen, Tirza, Bentwich, Zvi, Mozes, Edna

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