Korostishevsky M - 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. Among authors: korostishevsky m. 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

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. Among authors: korostishevsky m. Genomics. 1994 Mar 1;20(1):36-42. doi: 10.1006/geno.1994.1124. Genomics. 1994. PMID: 8020954

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. Among authors: korostishevsky m. 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. Among authors: korostishevsky m. 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. Among authors: korostishevsky m. 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. Among authors: korostishevsky m. 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. Among authors: korostishevsky m. 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

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. Tamary H, et al. Among authors: korostishevsky m. Am J Hum Genet. 1998 May;62(5):1062-9. doi: 10.1086/301834. Am J Hum Genet. 1998. PMID: 9545404 Free PMC article.

9

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 HS, 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. Berry A, et al. Among authors: korostishevsky m. Genomics. 2000 Aug 15;68(1):22-9. doi: 10.1006/geno.2000.6253. Genomics. 2000. PMID: 10950923

10

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 KK, Bonne-Tamir B. Iyengar S, et al. Among authors: korostishevsky m. J Med Genet. 1997 May;34(5):391-4. doi: 10.1136/jmg.34.5.391. J Med Genet. 1997. PMID: 9152836 Free PMC article.

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