Abeliovich D - Search Results

1

Analysis of four diverse population groups indicates that a subset of cystic fibrosis mutations occur in common among Caucasians.

Cutting GR, Curristin SM, Nash E, Rosenstein BJ, Lerer I, Abeliovich D, Hill A, Graham C. Cutting GR, et al. Among authors: abeliovich d. Am J Hum Genet. 1992 Jun;50(6):1185-94. Am J Hum Genet. 1992. PMID: 1376017 Free PMC article.

2

Cystic fibrosis mutations delta F508 and G542X in Jewish patients.

Lerer I, Sagi M, Cutting GR, Abeliovich D. Lerer I, et al. Among authors: abeliovich d. J Med Genet. 1992 Feb;29(2):131-3. doi: 10.1136/jmg.29.2.131. J Med Genet. 1992. PMID: 1377276 Free PMC article.

3

Screening for five mutations detects 97% of cystic fibrosis (CF) chromosomes and predicts a carrier frequency of 1:29 in the Jewish Ashkenazi population.

Abeliovich D, Lavon IP, Lerer I, Cohen T, Springer C, Avital A, Cutting GR. Abeliovich D, et al. Am J Hum Genet. 1992 Nov;51(5):951-6. Am J Hum Genet. 1992. PMID: 1384328 Free PMC article.

4

The frequency of the delta F508 mutation on cystic fibrosis chromosomes in Israeli families: correlation to CF haplotypes in Jewish communities and Arabs.

Lerer I, Cohen S, Chemke M, Sanilevich A, Rivlin J, Golan A, Yahav J, Friedman A, Abeliovich D. Lerer I, et al. Among authors: abeliovich d. Hum Genet. 1990 Sep;85(4):416-7. doi: 10.1007/BF02428288. Hum Genet. 1990. PMID: 1976595

5

Cystic fibrosis heterozygote screening in the Orthodox Community of Ashkenazi Jews: the Dor Yesharim approach and heterozygote frequency.

Abeliovich D, Quint A, Weinberg N, Verchezon G, Lerer I, Ekstein J, Rubinstein E. Abeliovich D, et al. Eur J Hum Genet. 1996;4(6):338-41. doi: 10.1159/000472229. Eur J Hum Genet. 1996. PMID: 9043867

6

A large deletion mutation in the CFTR gene (3120+1Kbdel8.6Kb): a founder mutation in the Palestinian Arabs. Mutation in brief no. 231. Online.

Lerer I, Laufer-Cahana A, Rivlin JR, Augarten A, Abeliovich D. Lerer I, et al. Among authors: abeliovich d. Hum Mutat. 1999;13(4):337. doi: 10.1002/(SICI)1098-1004(1999)13:4<337::AID-HUMU13>3.0.CO;2-C. Hum Mutat. 1999. PMID: 10220150

7

Cystic fibrosis mutations in Israeli Arab patients.

Laufer-Cahana A, Lerer I, Sagi M, Rachmilewitz-Minei T, Zamir C, Rivlin JR, Abeliovich D. Laufer-Cahana A, et al. Among authors: abeliovich d. Hum Mutat. 1999 Dec;14(6):543. doi: 10.1002/(SICI)1098-1004(199912)14:6<543::AID-HUMU16>3.0.CO;2-V. Hum Mutat. 1999. PMID: 10571955

8

The 28-kb deletion spanning D15S63 is a polymorphic variant in the Ashkenazi Jewish population.

Silverstein S, Lerer I, Buiting K, Abeliovich D. Silverstein S, et al. Among authors: abeliovich d. Am J Hum Genet. 2001 Jan;68(1):261-3. doi: 10.1086/316943. Epub 2000 Nov 17. Am J Hum Genet. 2001. PMID: 11083946 Free PMC article.

9

Homozygosity for Waardenburg syndrome.

Zlotogora J, Lerer I, Bar-David S, Ergaz Z, Abeliovich D. Zlotogora J, et al. Among authors: abeliovich d. Am J Hum Genet. 1995 May;56(5):1173-8. Am J Hum Genet. 1995. PMID: 7726174 Free PMC article.

10

Neurofibromatosis type I (NFI) in Israeli families: linkage analysis as a diagnostic tool.

Elyakim S, Lerer I, Zlotogora J, Sagi M, Gelman-Kohan Z, Merin S, Abeliovich D. Elyakim S, et al. Among authors: abeliovich d. Am J Med Genet. 1994 Dec 1;53(4):325-34. doi: 10.1002/ajmg.1320530405. Am J Med Genet. 1994. PMID: 7864041

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