Bonne-Tamir B - Search Results

1

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 LA, Bonne-Tamir B. Kalinsky H, et al. Hum Mutat. 1998;11(2):145-51. doi: 10.1002/(SICI)1098-1004(1998)11:2<145::AID-HUMU7>3.0.CO;2-I. Hum Mutat. 1998. PMID: 9482578

2

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

Bonné-Tamir B, Frydman M, Agger MS, Bekeer R, Bowcock AM, Hebert JM, Cavalli-Sforza LL, Farrer LA. Bonné-Tamir B, et al. Ann Hum Genet. 1990 May;54(2):155-68. doi: 10.1111/j.1469-1809.1990.tb00372.x. Ann Hum Genet. 1990. PMID: 2382969

3

Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population.

Baldwin CT, Weiss S, Farrer LA, De Stefano AL, Adair R, Franklyn B, Kidd KK, Korostishevsky M, Bonné-Tamir B. Baldwin CT, et al. Hum Mol Genet. 1995 Sep;4(9):1637-42. doi: 10.1093/hmg/4.9.1637. Hum Mol Genet. 1995. PMID: 8541853

4

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

Bonné-Tamir B, DeStefano AL, Briggs CE, Adair R, Franklyn B, Weiss S, Korostishevsky M, Frydman M, Baldwin CT, Farrer LA. Bonné-Tamir B, et al. Am J Hum Genet. 1996 Jun;58(6):1254-9. Am J Hum Genet. 1996. PMID: 8651303 Free PMC article.

5

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

Adato A, Weil D, Kalinski H, Pel-Or Y, Ayadi H, Petit C, Korostishevsky M, Bonne-Tamir B. Adato A, et al. Am J Hum Genet. 1997 Oct;61(4):813-21. doi: 10.1086/514899. Am J Hum Genet. 1997. PMID: 9382091 Free PMC article.

6

Usher syndrome in the Samaritans: strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders.

Bonné-Tamir B, Nystuen A, Seroussi E, Kalinsky H, Kwitek-Black AE, Korostishevsky M, Adato A, Sheffield VC. Bonné-Tamir B, et al. Am J Phys Anthropol. 1997 Oct;104(2):193-200. doi: 10.1002/(SICI)1096-8644(199710)104:2<193::AID-AJPA5>3.0.CO;2-#. Am J Phys Anthropol. 1997. PMID: 9386826

7

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

Bonné-Tamir B, Korostishevsky M, Redd AJ, Pel-Or Y, Kaplan ME, Hammer MF. Bonné-Tamir B, et al. Ann Hum Genet. 2003 Mar;67(Pt 2):153-64. doi: 10.1046/j.1469-1809.2003.00024.x. Ann Hum Genet. 2003. PMID: 12675690

8

Genetic mapping of the gene for Usher syndrome: linkage analysis in a large Samaritan kindred.

Bonné-Tamir B, Korostishevsky M, Kalinsky H, Seroussi E, Beker R, Weiss S, Godel V. Bonné-Tamir B, et al. Genomics. 1994 Mar 1;20(1):36-42. doi: 10.1006/geno.1994.1124. Genomics. 1994. PMID: 8020954

9

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

Bowcock AM, Tomfohrde J, Weissenbach J, Bonne-Tamir B, St George-Hyslop P, Giagheddu M, Cavalli-Sforza LL, Farrer LA. Bowcock AM, et al. Am J Hum Genet. 1994 Jan;54(1):79-87. Am J Hum Genet. 1994. PMID: 8279473 Free PMC article.

10

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

Bowcock AM, Farrer LA, Cavalli-Sforza LL, Hebert JM, Kidd KK, Frydman M, Bonne-Tamir B. Bowcock AM, et al. Am J Hum Genet. 1987 Jul;41(1):27-35. Am J Hum Genet. 1987. PMID: 3474893 Free PMC article.

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