Human heme oxygenase cDNA and induction of its mRNA by hemin
YOSHIDA, Tadashi, BIRO, Peter, COHEN, Tirza, MÜLLER, Rita M., SHIBAHARA, Shigeki
Published in European journal of biochemistry (01.02.1988)
Published in European journal of biochemistry (01.02.1988)
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Sensorineural hearing loss in Jewish children born in Jerusalem
Levi, Haya, Tell, Lilly, Cohen, Tirza
Published in International journal of pediatric otorhinolaryngology (01.10.2004)
Published in International journal of pediatric otorhinolaryngology (01.10.2004)
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Diaphragmatic defects in children of consanguineous parents
Arad, I, Lijovetzky, G C, Starinsky, R, Laufer, N, Cohen, T
Published in Human genetics (01.08.1980)
Published in Human genetics (01.08.1980)
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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
ABELIOVICH, D, LAVON, I. P, LERER, I, COHEN, T, SPRINGER, C, AVITAL, A, CUTTING, G. R
Published in American journal of human genetics (01.11.1992)
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Published in American journal of human genetics (01.11.1992)
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HLA-DRw4 in pemphigus vulgaris patients in Israel
Brautbar, C, Moscovitz, M, Livshits, T, Haim, S, Hacham-Zadeh, S, Cohen, H A, Sharon, R, Nelken, D, Cohen, T
Published in Tissue antigens (01.09.1980)
Published in Tissue antigens (01.09.1980)
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Mutations in PAX3 associated with Waardenburg syndrome type I
Baldwin, C T, Lipsky, N R, Hoth, C F, Cohen, T, Mamuya, W, Milunsky, A
Published in Human mutation (1994)
Published in Human mutation (1994)
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Evolution of a Genetic Disease in an Ethnic Isolate: β-Thalassemia in the Jews of Kurdistan
Rund, Deborah, Cohen, Tirza, Filon, Dvora, Dowling, Carol E., Warren, Tina C., Barak, Igal, Rachmilewitz, Eliezer, Kazazian, Haig H., Oppenheim, Ariella
Published in Proceedings of the National Academy of Sciences - PNAS (01.01.1991)
Published in Proceedings of the National Academy of Sciences - PNAS (01.01.1991)
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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
SHIBAHARA, S, TAGUCHI, H, MULLER, R. M, SHIBATA, K, COHEN, T, TOMITA, Y, TAGAMI, H
Published in The Journal of biological chemistry (1991)
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Published in The Journal of biological chemistry (1991)
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A syndrome including thumb malformations, microcephaly, short stature, and hypogonadism
Zlotogora, J, Dagan, J, Ganen, A, Abu-Libdeh, M, Ben-Neriah, Z, Cohen, T
Published in Journal of medical genetics (01.10.1997)
Published in Journal of medical genetics (01.10.1997)
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The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22–q23
Ziv, Yael, Rotman, Galit, Frydman, Moshe, Dagan, Judith, Cohen, Tirza, Foroud, Tatiana, Gatti, Richard A., Shiloh, Yosef
Published in Genomics (San Diego, Calif.) (01.02.1991)
Published in Genomics (San Diego, Calif.) (01.02.1991)
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Syndrome of brittle cornea, blue sclera, and joint hyperextensibility
Zlotogora, J, BenEzra, D, Cohen, T, Cohen, E
Published in American journal of medical genetics (01.07.1990)
Published in American journal of medical genetics (01.07.1990)
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Familial hereditary thrombocytopenia and HLA
Naparstek, Y, Abrahamov, A, Cohen, T, Brautbar, C
Published in American journal of hematology (01.09.1984)
Published in American journal of hematology (01.09.1984)
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Clinical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency
Rösler, A, Leiberman, E, Sack, J, Landau, H, Benderly, A, Moses, S W, Cohen, T
Published in Hormone research (01.01.1982)
Published in Hormone research (01.01.1982)
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Hypodontia: A Polygenic Trait-A Family Study among Israeli Jews
Chosack, Aubrey, Eidelman, Eliecer, Cohen, Tirza
Published in Journal of dental research (01.01.1975)
Published in Journal of dental research (01.01.1975)
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