Lerer I - Search Results

1

Negative expansion of the myotonic dystrophy unstable sequence.

Abeliovich D, Lerer I, Pashut-Lavon I, Shmueli E, Raas-Rothschild A, Frydman M. Abeliovich D, et al. Among authors: lerer i. Am J Hum Genet. 1993 Jun;52(6):1175-81. Am J Hum Genet. 1993. PMID: 8503449 Free PMC article.

2

Myotonic dystrophy: molecular analysis of Israeli patients.

Abeliovich D, Lerer I, Pashut-Lavon I, Cohen T. Abeliovich D, et al. Among authors: lerer i. Biomed Pharmacother. 1994;48(8-9):373-80. doi: 10.1016/0753-3322(94)90054-x. Biomed Pharmacother. 1994. PMID: 7858174

3

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: lerer i. Am J Med Genet. 1994 Dec 1;53(4):325-34. doi: 10.1002/ajmg.1320530405. Am J Med Genet. 1994. PMID: 7864041

4

Molecular diagnosis of Prader-Willi syndrome: parent-of-origin dependent methylation sites and non-isotopic detection of (CA)n dinucleotide repeat polymorphisms.

Lerer I, Meiner V, Pashut-Lavon I, Abeliovich D. Lerer I, et al. Am J Med Genet. 1994 Aug 1;52(1):79-84. doi: 10.1002/ajmg.1320520116. Am J Med Genet. 1994. PMID: 7977468

5

Prevalence of myotonic dystrophy in Israeli Jewish communities: inter-community variation and founder premutations.

Segel R, Silverstein S, Lerer I, Kahana E, Meir R, Sagi M, Zilber N, Korczyn AD, Shapira Y, Argov Z, Abeliovich D. Segel R, et al. Among authors: lerer i. Am J Med Genet A. 2003 Jun 15;119A(3):273-8. doi: 10.1002/ajmg.a.20177. Am J Med Genet A. 2003. PMID: 12784291

6

Deletion of the ANKRD15 gene at 9p24.3 causes parent-of-origin-dependent inheritance of familial cerebral palsy.

Lerer I, Sagi M, Meiner V, Cohen T, Zlotogora J, Abeliovich D. Lerer I, et al. Hum Mol Genet. 2005 Dec 15;14(24):3911-20. doi: 10.1093/hmg/ddi415. Epub 2005 Nov 21. Hum Mol Genet. 2005. PMID: 16301218

7

The H syndrome is caused by mutations in the nucleoside transporter hENT3.

Molho-Pessach V, Lerer I, Abeliovich D, Agha Z, Abu Libdeh A, Broshtilova V, Elpeleg O, Zlotogorski A. Molho-Pessach V, et al. Among authors: lerer i. Am J Hum Genet. 2008 Oct;83(4):529-34. doi: 10.1016/j.ajhg.2008.09.013. Am J Hum Genet. 2008. PMID: 18940313 Free PMC article.

8

Cystic fibrosis mutations delta F508 and G542X in Jewish patients.

Lerer I, Sagi M, Cutting GR, Abeliovich D. Lerer I, et al. 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.

9

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. Among authors: lerer i. Am J Hum Genet. 1992 Nov;51(5):951-6. Am J Hum Genet. 1992. PMID: 1384328 Free PMC article.

10

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. Hum Genet. 1990 Sep;85(4):416-7. doi: 10.1007/BF02428288. Hum Genet. 1990. PMID: 1976595

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