Analysis of biochemical genetic data on Jewish populations. III. The application of individual phenotype measurements for population comparisons.

Por Karlin, S, Carmelli, D, Bonné-Tamir, B
Publicado em 1982

Analysis of genetic data on Jewish populations. I. Historical background, demographic features, and genetic markers.

Por Bonné-Tamir, B, Karlin, S, Kenett, R
Publicado em 1979

Analysis of biochemical genetic data on Jewish populations: II. Results and interpretations of heterogeneity indices and distance measures with respect to standards.

Por Karlin, S, Kenett, R, Bonné-Tamir, B
Publicado em 1979

The inheritance of fingerprint patterns.

Por Slatis, H M, Katznelson, M B, Bonné-Tamir, B
Publicado em 1976

Linkage analysis and the inheritance of arches in a Habbanite isolate.

Por Anderson, M W, Bonné-Tamir, B, Carmelli, D, Thompson, E A
Publicado em 1979

Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance.

Por Adato, A, Kalinski, H, Weil, D, Chaib, H, Korostishevsky, M, Bonne-Tamir, B
Publicado em 1999

Human mitochondrial DNA types in two Israeli populations--a comparative study at the DNA level.

Por Bonné-Tamir, B, Johnson, M J, Natali, A, Wallace, D C, Cavalli-Sforza, L L
Publicado em 1986

Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus.

Por Frydman, M, Bonné-Tamir, B, Farrer, L A, Conneally, P M, Magazanik, A, Ashbel, S, Goldwitch, Z
Publicado em 1985

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

Por Iyengar, S, Kalinsky, H, Weiss, S, Korostishevsky, M, Sadeh, M, Zhao, Y, Kidd, K K, Bonne-Tamir, B
Publicado em 1997

Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins.

Por Adato, A, Weil, D, Kalinski, H, Pel-Or, Y, Ayadi, H, Petit, C, Korostishevsky, M, Bonne-Tamir, B
Publicado em 1997

The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs.

Por Macaulay, V, Richards, M, Hickey, E, Vega, E, Cruciani, F, Guida, V, Scozzari, R, Bonné-Tamir, B, Sykes, B, Torroni, A
Publicado em 1999

Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.

Por Bowcock, A M, Farrer, L A, Cavalli-Sforza, L L, Hebert, J M, Kidd, K K, Frydman, M, Bonne-Tamir, B
Publicado em 1987

Medical genetics in Israel.

Por Goodman, R M, Bonne-Tamir, B, Adam, A, Voss, R, Bach, G, Shiloh, Y, Katznelson, M B, Barkai, G, Goldman, B, Padeh, B
Publicado em 1989

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

Por Tamary, H, Shalmon, L, Shalev, H, Halil, A, Dobrushin, D, Ashkenazi, N, Zoldan, M, Resnitzky, P, Korostishevsky, M, Bonne-Tamir, B, Zaizov, R
Publicado em 1998

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

Por Bowcock, A. M., Tomfohrde, J., Weissenbach, J., Bonne-Tamir, B., St George-Hyslop, P., Giagheddu, M., Cavalli-Sforza, L. L., Farrer, L. A.
Publicado em 1994

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

Por 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
Publicado em 1998

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

Por Bonné-Tamir, B., DeStefano, A. L., Briggs, C. E., Adair, R., Franklyn, B., Weiss, S., Korostishevsky, M., Frydman, M., Baldwin, C. T., Farrer, L. A.
Publicado em 1996

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

Por 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
Publicado em 1998

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

Por 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.
Publicado em 2000

Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness

Por Ben-Yosef, T., Wattenhofer, M., Riazuddin, S., Ahmed, Z., Scott, H., Kudoh, J., Shibuya, K., Antonarakis, S., Bonne-Tamir, B., Radhakrishna, U., Naz, S., Ahmed, Z., Riazuddin, S., Pandya, A., Nance, W., Wilcox, E., Friedman, T., Morell, R.
Publicado em 2001