Batsheva Bonne-Tamir

2010

The genome-wide structure of the Jewish people

Behar, D. M., Yunusbayev, B., Metspalu, M., Metspalu, E., Rosset, S., Parik, J., Rootsi, S., Chaubey, G., Kutuev, I., Yudkovsky, G., Khusnutdinova, E. K., Balanovsky, O., Semino, O., Pereira, L., Comas, D., Gurwitz, D., Bonne-Tamir, B., Parfitt, T., Hammer, M. F. & Skorecki, K. & 1 others, Villems, R., 8 Jul 2010, In: Nature. 466, 7303, p. 238-242 5 p.

Research output: Contribution to journal › Article › peer-review

317 Scopus citations

2008

Counting the founders: The matrilineal genetic ancestry of the Jewish Diaspora

Behar, D. M., Metspalu, E., Kivisilid, T., Rosset, S., Tzur, S., Hadid, Y., Yudkovsky, G., Rosengarten, D., Pereira, L., Amorim, A., Kutuev, I., Gurwitz, D., Bonne-Tamir, B., Villems, R. & Skorecki, K., 30 Apr 2008, In: PLoS ONE. 3, 4, e2062.

Research output: Contribution to journal › Article › peer-review

Open Access

97 Scopus citations

2006

The matrilineal ancestry of Ashkenazi Jewry: Portrait of a recent founder event

Behar, D. M., Metspalu, E., Kivisild, T., Achilli, A., Hadid, Y., Tzur, S., Pereira, L., Amorim, A., Quintana-Murci, L., Majamaa, K., Herrnstadt, C., Howell, N., Balanovsky, O., Kutuev, I., Pshenichnov, A., Gurwitz, D., Bonne-Tamir, B., Torroni, A., Villems, R. & Skorecki, K., Mar 2006, In: American Journal of Human Genetics. 78, 3, p. 487-497 11 p.

Research output: Contribution to journal › Article › peer-review

Open Access

129 Scopus citations

2005

Considerable haplotype diversity within the 23kb encompassing the ADH7 gene

Han, Y., Oota, H., Osier, M. V., Pakstis, A. J., Speed, W. C., Odunsi, A., Okonofua, F., Kajuna, S. L. B., Karoma, N. J., Kungulilo, S., Grigorenko, E., Zhukova, O. V., Bonne-Tamir, B., Lu, R. B., Parnas, J., Schulz, L. O., Kidd, J. R. & Kidd, K. K., Dec 2005, In: Alcoholism: Clinical and Experimental Research. 29, 12, p. 2091-2100 10 p.

Research output: Contribution to journal › Article › peer-review

19 Scopus citations

Mechanisms of Ageing and Development: Preface

Bonne-Tamir, B., Feb 2005, In: Mechanisms of Ageing and Development. 126, 2, p. 223 1 p.

Research output: Contribution to journal › Article › peer-review

2004

COMT haplotypes suggest P2 promoter region relevance for schizophrenia

Palmatier, M. A., Pakstis, A. J., Speed, W., Paschou, P., Goldman, D., Odunsi, A., Okonofua, F., Kajuna, S., Karoma, N., Kungulilo, S., Grigorenko, E., Zhukova, O. V., Bonne-Tamir, B., Lu, R. B., Parnas, J., Kidd, J. R., DeMille, M. M. C. & Kidd, K. K., Sep 2004, In: Molecular Psychiatry. 9, 9, p. 859-870 12 p.

Research output: Contribution to journal › Article › peer-review

68 Scopus citations

MtDNA evidence for a genetic bottleneck in the early history of the Ashkenazi Jewish population

Behar, D. M., Hammer, M. F., Garrigan, D., Villems, R., Bonne-Tamir, B., Richards, M., Gurwitz, D., Rosengarten, D., Kaplan, M., Della Pergola, S., Quintana-Murci, L. & Skorecki, K., May 2004, In: European Journal of Human Genetics. 12, 5, p. 355-364 10 p.

Research output: Contribution to journal › Article › peer-review

Open Access

73 Scopus citations

The evolution and population genetics of the ALDH2 locus: Random genetic drift, selection, and low levels of recombination

Oota, H., Pakstis, A. J., Bonne-Tamir, B., Goldman, D., Grigorenko, E., Kajuna, S. L. B., Karoma, N. J., Kungulilo, S., Lu, R. B., Odunsi, K., Okonofua, F., Zhukova, O. V., Kidd, J. R. & Kidd, K. K., Mar 2004, In: Annals of Human Genetics. 68, 2, p. 93-109 17 p.

Research output: Contribution to journal › Article › peer-review

126 Scopus citations

2003

Global survey of haplotype frequencies and linkage disequilibrium at the RET locus

Chattopadhyay, P., Pakstis, A. J., Mukherjee, N., Iyengar, S., Odunsi, A., Okonofua, F., Bonne-Tamir, B., Speed, W., Kidd, J. R. & Kidd, K. K., Oct 2003, In: European Journal of Human Genetics. 11, 10, p. 760-769 10 p.

Research output: Contribution to journal › Article › peer-review

Open Access

14 Scopus citations

Maternal and paternal lineages of the Samaritan isolate: Mutation rates and time to most recent common male ancestor

Bonné-Tamir, B., Korostishevsky, M., Redd, A. J., Pel-Or, Y., Kaplan, M. E. & Hammer, M. F., Mar 2003, In: Annals of Human Genetics. 67, 2, p. 153-164 12 p.

Research output: Contribution to journal › Article › peer-review

21 Scopus citations

2002

A global perspective on genetic variation at the ADH genes reveals unusual patterns of linkage disequilibrium and diversity

Osier, M. V., Pakstis, A. J., Soodyall, H., Comas, D., Goldman, D., Odunsi, A., Okonofua, F., Parnas, J., Schulz, L. O., Bertranpetit, J., Bonne-Tamir, B., Lu, R. B., Kidd, J. R. & Kidd, K. K., 2002, In: American Journal of Human Genetics. 71, 1, p. 84-99 16 p.

Research output: Contribution to journal › Article › peer-review

Open Access

231 Scopus citations

Population variation in linkage disequilibrium across the COMT gene considering promoter region and coding region variation

DeMille, M. M. C., Kidd, J., Ruggeri, V., Palmatier, M. A., Goldman, D., Odunsi, A., Okonofua, F., Grigorenko, E., Schulz, L. O., Bonne-Tamir, B., Lu, R. B., Parnas, J., Pakstis, A. J. & Kidd, K. K., Dec 2002, In: Human Genetics. 111, 6, p. 521-537 17 p.

Research output: Contribution to journal › Article › peer-review

74 Scopus citations

USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses

Adato, A., Vreugde, S., Joensuu, T., Avidan, N., Hamalainen, R., Belenkiy, O., Olender, T., Bonne-Tamir, B., Ben-Asher, E., Espinos, C., Millán, J. M., Lehesjoki, A. E., Flannery, J. G., Avraham, K. B., Pietrokovski, S., Sankila, E. M., Beckmann, J. S. & Lancet, D., 2002, In: European Journal of Human Genetics. 10, 6, p. 339-350 12 p.

Research output: Contribution to journal › Article › peer-review

Open Access

144 Scopus citations

2001

Distinctive genetic signatures in the Libyan Jews

Rosenberg, N. A., Woolf, E., Pritchard, J. K., Schaap, T., Gefel, D., Shpirer, I., Lavi, U., Bonné-Tamir, B., Hillel, J. & Feldman, M. W., 30 Jan 2001, In: Proceedings of the National Academy of Sciences of the United States of America. 98, 3, p. 858-863 6 p.

Research output: Contribution to journal › Article › peer-review

Open Access

37 Scopus citations

Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness

Scott, H. S., Kudoh, J., Wattenhofer, M., Shibuya, K., Berry, A., Chrast, R., Guipponi, M., Wang, J., Kawasaki, K., Asakawa, S., Minoshima, S., Younus, F., Mehdi, S. Q., Radhakrishna, U., Papasavvas, M. P., Gehrig, C., Rossier, C., Korostishevsky, M., Gal, A. & Shimizu, N. & 2 others, Bonne-Tamir, B. & Antonarakis, S. E., 2001, In: Nature Genetics. 27, 1, p. 59-63 5 p.

Research output: Contribution to journal › Article › peer-review

Open Access

200 Scopus citations

Isolation and characterization of the UBASH3A gene on 21q22.3 encoding a potential nuclear protein with a novel combination of domains

Wattenhofer, M., Shibuya, K., Kudoh, J., Lyle, R., Michaud, J., Rossier, C., Kawasaki, K., Asakawa, S., Minoshima, S., Berry, A., Bonne-Tamir, B., Shimizu, N., Antonarakis, S. E. & Scott, H. S., 2001, In: Human Genetics. 108, 2, p. 140-147 8 p.

Research output: Contribution to journal › Article › peer-review

46 Scopus citations

Worldwide genetic analysis of the CFTR region

Mateu, E., Calafell, F., Lao, O., Bonné-Tamir, B., Kidd, J. R., Pakstis, A., Kidd, K. K. & Bertranpetit, J., 2001, In: American Journal of Human Genetics. 68, 1, p. 103-117 15 p.

Research output: Contribution to journal › Article › peer-review

Open Access

46 Scopus citations

2000

Cloning and characterization of a putative human glycerol 3-phosphate permease gene (SLC37A1 or G3PP) on 21q22.3: Mutation analysis in two candidate phenotypes, DFNB10 and a glycerol kinase deficiency

Bartoloni, L., Wattenhofer, M., Kudoh, J., Berry, A., Shibuya, K., Kawasaki, K., Wang, J., Asakawa, S., Talior, I., Bonne-Tamir, B., Rossier, C., Michaud, J., McCabe, E. R. B., Minoshima, S., Shimizu, N., Scott, H. S. & Antonarakis, S. E., 1 Dec 2000, In: Genomics. 70, 2, p. 190-200 11 p.

Research output: Contribution to journal › Article › peer-review

29 Scopus citations

Deafness heterogeneity in a Druze isolate from the Middle East: Novel OTOF and PDS mutations, low prevalence of GJB2 35delG mutation and indication for a new DFNB locus

Adato, A., Raskin, L., Petit, C. & Bonne-Tamir, B., Jun 2000, In: European Journal of Human Genetics. 8, 6, p. 437-442 6 p.

Research output: Contribution to journal › Article › peer-review

Open Access

43 Scopus citations

Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations

Kidd, J. R., Pakstis, A. J., Zhao, H., Lu, R. B., Okonofua, F. E., Odunsi, A., Grigorenko, E., Bonne-Tamir, B., Friedlaender, J., Schulz, L. O., Parnas, J. & Kidd, K. K., 2000, In: American Journal of Human Genetics. 66, 6, p. 1882-1899 18 p.

Research output: Contribution to journal › Article › peer-review

Open Access

128 Scopus citations

Isolation and characterization of a human chromosome 21q22.3 gene (WDR4) and its mouse homologue that code for a WD-repeat protein

Michaud, J., Kudoh, J., Berry, A., Bonne-Tamir, B., Lalioti, M. D., Rossier, C., Shibuya, K., Kawasaki, K., Asakawa, S., Minoshima, S., Shimizu, N., Antonarakis, S. E. & Scott, H. S., 15 Aug 2000, In: Genomics. 68, 1, p. 71-79 9 p.

Research output: Contribution to journal › Article › peer-review

50 Scopus citations

Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes

Hammer, M. F., Redd, A. J., Wood, E. T., Bonner, M. R., Jarjanazi, H., Karafet, T., Santachiara-Benerecetti, S., Oppenheim, A., Jobling, M. A., Jenkins, T., Ostrer, H. & Bonné-Tamir, B., 6 Jun 2000, In: Proceedings of the National Academy of Sciences of the United States of America. 97, 12, p. 6769-6774 6 p.

Research output: Contribution to journal › Article › peer-review

Open Access

221 Scopus citations

Refined localization of autosomal recessive nonsyndromic deafness DFNB10 locus using 34 novel microsatellite markers, genomic structure, and exclusion of six known genes in the region

Berry, A., Scott, H. S., Kudoh, J., Talior, I., Korostishevsky, M., Wattenhofer, M., Guipponi, M., Barras, C., Rossier, C., Shibuya, K., Wang, J., Kawasaki, K., Asakawa, S., Minoshima, S., Shimizu, N., Antonarakis, S. & Bonné-Tamir, B., 15 Aug 2000, In: Genomics. 68, 1, p. 22-29 8 p.

Research output: Contribution to journal › Article › peer-review

20 Scopus citations

Y chromosome sequence variation and the history of human populations

Underhill, P. A., Shen, P., Lin, A. A., Jin, L., Passarino, G., Yang, W. H., Kauffman, E., Bonné-Tamir, B., Bertranpetit, J., Francalacci, P., Ibrahim, M., Jenkins, T., Kidd, J. R., Mehdi, S. Q., Seielstad, M. T., Wells, R. S., Piazza, A., Davis, R. W., Feldman, M. W. & Cavalli-Sforza, L. L. & 1 others, Oefner, P. J., 2000, In: Nature Genetics. 26, 3, p. 358-361 4 p.

Research output: Contribution to journal › Article › peer-review

790 Scopus citations

1999

Allele frequencies in a worldwide survey of a CA repeat in the first intron of the CFTR gene

Mateu, E., Calafell, F., Bonné-Tamir, B., Kidd, J. R., Casals, T., Kidd, K. K. & Bertranpetit, J., Jan 1999, In: Human Heredity. 49, 1, p. 15-20 6 p.

Research output: Contribution to journal › Article › peer-review

13 Scopus citations

Genetic variation of three tetrameric tandem repeats in four distinct Israeli ethnic groups

Amar, A., Brautbar, C., Motro, U., Fisher, T., Bonne-Tamir, B. & Israel, S., Sep 1999, In: Journal of Forensic Sciences. 44, 5, p. 983-986 4 p.

Research output: Contribution to journal › Article › peer-review

15 Scopus citations

Molecular analysis of HLA class II polymorphisms among different ethnic groups in Israel

Amar, A., Kwon, O. J., Motro, U., Witt, C. S., Bonne-Tamir, B., Gabison, R. & Brautbar, C., Aug 1999, In: Human Immunology. 60, 8, p. 723-730 8 p.

Research output: Contribution to journal › Article › peer-review

48 Scopus citations

The emerging tree of west Eurasian mtDNAs: A synthesis of control-region sequences and RFLPs

Macaulay, V., Richards, M., Hickey, E., Vega, E., Cruciani, F., Guida, V., Scozzari, R., Bonné-Tamir, B., Sykes, B. & Torroni, A., 1999, In: American Journal of Human Genetics. 64, 1, p. 232-249 18 p.

Research output: Contribution to journal › Article › peer-review

Open Access

513 Scopus citations

The HGDP can be and should be pursued in harmony with its subjects: An account of the Israeli experience

Bonné-Tamir, B., 1999, In: Politics and the Life Sciences. 18, 2, p. 291-293 3 p.

Research output: Contribution to journal › Article › peer-review

1 Scopus citations

1998

A global haplotype analysis of the myotonic dystrophy locus: Implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations

Tishkoff, S. A., Goldman, A., Calafell, F., Speed, W. C., Deinard, A. S., Bonne-Tamir, B., Kidd, J. R., Pakstis, A. J., Jenkins, T. & Kidd, K. K., Jun 1998, In: American Journal of Human Genetics. 62, 6, p. 1389-1402 14 p.

Research output: Contribution to journal › Article › peer-review

Open Access

160 Scopus citations

A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus

Kidd, K. K., Morar, B., Castiglione, C. M., Zhao, H., Pakstis, A. J., Speed, W. C., Bonne-Tamir, B., Lu, R. B., Goldman, D., Lee, C., Nam, Y. S., Grandy, D. K., Jenkins, T. & Kidd, J. R., 1998, In: Human Genetics. 103, 2, p. 211-227 17 p.

Research output: Contribution to journal › Article › peer-review

167 Scopus citations

Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3

Tamary, H., Shalmon, L., Shalev, H., Halil, A., Dobrushin, D., Ashkenazi, N., Zoldan, M., Resnitzky, P., Korostishevsky, M., Bonne-Tamir, B. & Zaizov, R., May 1998, In: American Journal of Human Genetics. 62, 5, p. 1062-1069 8 p.

Research output: Contribution to journal › Article › peer-review

Open Access

53 Scopus citations

mtDNA analysis reveals a major late paleolithic population expansion from southwestern to northeastern Europe

Torroni, A., Bandelt, H. J., D'Urbano, L., Lahermo, P., Moral, P., Sellitto, D., Rengo, C., Forster, P., Savontaus, M. L., Bonné-Tamir, B. & Scozzari, R., May 1998, In: American Journal of Human Genetics. 62, 5, p. 1137-1152 16 p.

Research output: Contribution to journal › Article › peer-review

Open Access

296 Scopus citations

Novel ATP7B mutations causing Wilson disease in several Israeli ethnic groups

Kalinsky, H., Funes, A., Zeldin, A., Pel-Or, Y., Korostishevsky, M., Gershoni-Baruch, R., Farrer, L. A. & Bonne-Tamir, B., 1998, In: Human Mutation. 11, 2, p. 145-151 7 p.

Research output: Contribution to journal › Article › peer-review

Open Access

50 Scopus citations

1997

Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease

Iyengar, S., Kalinsky, H., Weiss, S., Korostishevsky, M., Sadeh, M., Zhao, Y., Kidd, K. K. & Bonne-Tamir, B., 1997, In: Journal of Medical Genetics. 34, 5, p. 391-394 4 p.

Research output: Contribution to journal › Article › peer-review

Open Access

6 Scopus citations

Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase gene

Nystuen, A., Costeff, H., Elpeleg, O. N., Apter, N., Bonné-Tamir, B., Mohrenweiser, H., Haider, N., Stone, E. M. & Sheffield, V. C., Apr 1997, In: Human Molecular Genetics. 6, 4, p. 563-569 7 p.

Research output: Contribution to journal › Article › peer-review

Open Access

24 Scopus citations

1996

DRD2 haplotypes containing the taqI A1 allele: Implications for alcoholism research

Kidd, K. K., Pakstis, A. J., Castiglione, C. M., Kidd, J. R., Speed, W. C., Goldman, D., Knowler, W. C., Lu, R. B. & Bonne-Tamir, B., 1996, In: Alcoholism: Clinical and Experimental Research. 20, 4, p. 697-705 9 p.

Research output: Contribution to journal › Article › peer-review

59 Scopus citations

Global patterns of linkage disequilibrium at the CD4 locus and modern human origins

Tishkoff, S. A., Dietzsch, E., Speed, W., Pakstis, A. J., Kidd, J. R., Cheung, K., Bonne-Tamir, B., Santachiara-Benerecetti, A. S., Moral, P., Krings, M., Paabo, S., Watson, E., Risch, N., Jenkins, T. & Kidd, K. K., 8 Mar 1996, In: Science. 271, 5254, p. 1380-1387 8 p.

Research output: Contribution to journal › Article › peer-review

496 Scopus citations

Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3

Bonne-Tamir, B., DeStefano, A. L., Briggs, C. E., Adair, R., Franklyn, B., Weiss, S., Korostishevsky, M., Frydman, M., Baldwin, C. T. & Farrer, L. A., 1996, In: American Journal of Human Genetics. 58, 6, p. 1254-1259 6 p.

Research output: Contribution to journal › Article › peer-review

95 Scopus citations

1995

Evolution of haplotypes at the DRD2 locus

Castiglione, C. M., Deinard, A. S., Speed, W. C., Sirugo, G., Rosenbaum, H. C., Zhang, Y., Grandy, D. K., Grigorenko, E. L., Bonne-Tamir, B., Pakstis, A. J., Kidd, J. R. & Kidd, K. K., 1995, In: American Journal of Human Genetics. 57, 6, p. 1445-1456 12 p.

Research output: Contribution to journal › Article › peer-review

108 Scopus citations

Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the middle eastern druze population

Baldwin, C. T., Weiss, S., Farrer, L. A., De Stefano, A. L., Adair, R., Franklyn, B., Kidd, K. K., Korostishevsky, M. & Bonné-tamir, B., Sep 1995, In: Human Molecular Genetics. 4, 9, p. 1637-1642 6 p.

Research output: Contribution to journal › Article › peer-review

90 Scopus citations

1994

Genetic mapping of the gene for usher syndrome: Linkage analysis in a large samaritan kindred

Bonne-Tamir, B., Korostishevsky, M., Kalinsky, H., Seroussi, E., Beker, R., Weiss, S. & Godel, V., 1 Mar 1994, In: Genomics. 20, 1, p. 36-42 7 p.

Research output: Contribution to journal › Article › peer-review

25 Scopus citations

Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites

Bowcock, A. M., Tomfohrde, J., Weissenbach, J., Bonne-Tamir, B., St George-Hyslop, P., Giagheddu, M., Cavalli-Sforza, L. L. & Farrer, L. A., Jan 1994, In: American Journal of Human Genetics. 54, 1, p. 79-87 9 p.

Research output: Contribution to journal › Article › peer-review

27 Scopus citations

1993

Mitochondrial DNA affinity of several Jewish communities.

Ritte, U., Neufeld, E., Prager, E. M., Gross, M., Hakim, I., Khatib, A. & Bonné-Tamir, B., Jun 1993, In: Human Biology. 65, 3, p. 359-385 27 p.

Research output: Contribution to journal › Article › peer-review

41 Scopus citations

Polymorphic microsatellites and Wilson disease (WD)

Stewart, E. A., White, A., Tomfohrde, J., Osborne-Lawrence, S., Prestridge, L., Bonne-Tamir, B., Scheinberg, I. H., St George-Hyslop, P., Giagheddu, M., Kim, J. W., Seo, J. K., Lo, W. H. Y., Ivanova-Smolenskaya, I. A., Limborska, S. A., Cavalli-Sforza, L. L., Farrer, L. A. & Bowcock, A. M., Oct 1993, In: American Journal of Human Genetics. 53, 4, p. 864-873 10 p.

Research output: Contribution to journal › Article › peer-review

28 Scopus citations

1991

Assessment of the Hypothalamic‐Pituitary‐Testicular Function in Male Patients with Wilson's Disease

FRYDMAN, M., KAUSCHANSKY, A., BONNE‐TAMIR, B., NASSAR, F. & HOMBURG, R., 1991, In: Journal of Andrology. 12, 3, p. 180-184 5 p.

Research output: Contribution to journal › Article › peer-review

Open Access

13 Scopus citations

Genetic affinities of Ethiopian Jews

Zoossmann-Diskin, A., Ticher, A., Hakim, I., Goldwitch, Z., Rubinstein, A. & Bonne-Tamir, B., 1991, In: Israel Journal of Medical Sciences. 27, 5, p. 245-251 7 p.

Research output: Contribution to journal › Article › peer-review

18 Scopus citations

Predictive testing for wilson’s disease using tightly linked and flanking DNA markers

Farrer, L. A., Bowcock, A. M., Hebert, J. M., Bonné-Tamir, B., Sternlieb, I., Giagheddu, M., George-Hyslop, P. S., Frydman, M., Lössner, J., Demelia, L., Carcassi, C., Lee, R., Beker, R., Bale, A. E., Donis-Keller, H., Scheinberg, I. H. & Cavalli-Sforza, L. L., Jul 1991, In: Neurology. 41, 7, p. 992-999 8 p.

Research output: Contribution to journal › Article › peer-review

61 Scopus citations

1990

Wilson's disease in Israel: a genetic and epidemiological study

BONNÉ‐TAMIR, B., FRYDMAN, M., AGGER, M. S., BEKEER, R., BOWCOCK, A. M., HEBERT, J. M., CAVALLI‐SFORZA, L. L. & FARRER, L. A., May 1990, In: Annals of Human Genetics. 54, 2, p. 155-168 14 p.

Research output: Contribution to journal › Article › peer-review

34 Scopus citations

1989

Medical genetics in Isreal

Goodman, R. M., Bonne-Tamir, B., Adam, A., Voss, R., Bach, G., Shiloh, Y., Bat-Miriam Katznelson, M., Barkai, G., Goldman, B., Padeh, B., Chemke, J. & Legum, C., 1989, In: Journal of Medical Genetics. 26, 3, p. 179-189 11 p.

Research output: Contribution to journal › Article › peer-review

7 Scopus citations

Batsheva Bonne-Tamir

Research output

Search results