Lerer I - Search Results

1

A patient with Prader-Willi syndrome and a supernumerary marker chromosome r(15)(q11.1-13p11.1)pat and maternal heterodisomy.

Werner M, Ben-Neriah Z, Silverstein S, Lerer I, Dagan Y, Abeliovich D. Werner M, et al. Among authors: lerer i. Am J Med Genet A. 2004 Aug 30;129A(2):176-9. doi: 10.1002/ajmg.a.20621. Am J Med Genet A. 2004. PMID: 15316980

2

Uniparental disomy in fetuses diagnosed with balanced Robertsonian translocations: risk estimate.

Silverstein S, Lerer I, Sagi M, Frumkin A, Ben-Neriah Z, Abeliovich D. Silverstein S, et al. Among authors: lerer i. Prenat Diagn. 2002 Aug;22(8):649-51. doi: 10.1002/pd.370. Prenat Diagn. 2002. PMID: 12210570

3

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

4

t(15;21)(q15;q22.1) pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring.

Abeliovich D, Dagan J, Lerer I, Silberstein S, Katznelson MB, Frydman M. Abeliovich D, et al. Among authors: lerer i. Am J Med Genet. 1996 Dec 2;66(1):45-51. doi: 10.1002/(SICI)1096-8628(19961202)66:1<45::AID-AJMG10>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8957510

5

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: lerer i. 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.

6

Wiedemann-Beckwith syndrome: further prenatal characterization of the condition.

Reish O, Lerer I, Amiel A, Heyman E, Herman A, Dolfin T, Abeliovich D. Reish O, et al. Among authors: lerer i. Am J Med Genet. 2002 Jan 22;107(3):209-13. doi: 10.1002/ajmg.10143. Am J Med Genet. 2002. PMID: 11807901 Review.

7

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

8

Mutation spectrum in Jewish cystic fibrosis patients in Israel: implication to carrier screening.

Quint A, Lerer I, Sagi M, Abeliovich D. Quint A, et al. Among authors: lerer i. Am J Med Genet A. 2005 Jul 30;136(3):246-8. doi: 10.1002/ajmg.a.30823. Am J Med Genet A. 2005. PMID: 15948195

9

Paternal isodisomy of chromosome 7 with cystic fibrosis and overgrowth.

Fares F, David M, Lerner A, Diukman R, Lerer I, Abeliovich D, Rivlin J. Fares F, et al. Among authors: lerer i. Am J Med Genet A. 2006 Aug 15;140(16):1785-8. doi: 10.1002/ajmg.a.31380. Am J Med Genet A. 2006. PMID: 16835920

10

The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: report on two patients and review of the literature.

Raas-Rothschild A, Dijkhuizen T, Sikkema-Raddatz B, Werner M, Dagan J, Abeliovich D, Lerer I. Raas-Rothschild A, et al. Among authors: lerer i. Eur J Med Genet. 2009 Mar-Jun;52(2-3):140-4. doi: 10.1016/j.ejmg.2009.03.011. Epub 2009 Mar 26. Eur J Med Genet. 2009. PMID: 19328248 Review.

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