Bonne-Tamir B - Search Results

1

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.

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

Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease.

Farrer LA, Bonne-Tamir B, Frydman M, Magazanik A, Kidd KK, Bowcock AM, Cavalli-Sforza LL. Farrer LA, et al. Hum Genet. 1988 Jun;79(2):109-17. doi: 10.1007/BF00280547. Hum Genet. 1988. PMID: 3164701

4

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.

5

Polymorphic microsatellites and Wilson disease (WD).

Stewart EA, White A, Tomfohrde J, Osborne-Lawrence S, Prestridge L, Bonne-Tamir B, Scheinberg IH, St George-Hyslop P, Giagheddu M, Kim JW, et al. Stewart EA, et al. Am J Hum Genet. 1993 Oct;53(4):864-73. Am J Hum Genet. 1993. PMID: 8213814 Free PMC article.

6

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

7

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.

8

Predictive testing for Wilson's disease using tightly linked and flanking DNA markers.

Farrer LA, Bowcock AM, Hebert JM, Bonné-Tamir B, Sternlieb I, Giagheddu M, St George-Hyslop P, Frydman M, Lössner J, Demelia L, et al. Farrer LA, et al. Neurology. 1991 Jul;41(7):992-9. doi: 10.1212/wnl.41.7.992. Neurology. 1991. PMID: 2067662

9

Evidence for linkage between Wilson disease and esterase D in three kindreds: detection of linkage for an autosomal recessive disorder by the family study method.

Bonné-Tamir B, Farrer LA, Frydman M, Kanaaneh H. Bonné-Tamir B, et al. Genet Epidemiol. 1986;3(3):201-9. doi: 10.1002/gepi.1370030307. Genet Epidemiol. 1986. PMID: 3459695

10

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

Frydman M, Bonné-Tamir B, Farrer LA, Conneally PM, Magazanik A, Ashbel S, Goldwitch Z. Frydman M, et al. Proc Natl Acad Sci U S A. 1985 Mar;82(6):1819-21. doi: 10.1073/pnas.82.6.1819. Proc Natl Acad Sci U S A. 1985. PMID: 3856863 Free PMC article.

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