Abeliovich D - Search Results

1

Localization of two X-linked mental retardation (XLMR) genes to Xp: MRX37 gene at Xp22.31-p22.32 and a putative MRX gene on Xp22.11-p22.2.

Bar-David S, Lerer I, Sarfaty CK, Kohan ZG, Meiner V, Zlotogora J, Abeliovich D. Bar-David S, et al. Among authors: abeliovich d. Am J Med Genet. 1996 Jul 12;64(1):83-8. doi: 10.1002/(SICI)1096-8628(19960712)64:1<83::AID-AJMG15>3.0.CO;2-O. Am J Med Genet. 1996. PMID: 8826456

2

Paracentric inversion X(q21.2q24) associated with mental retardation in males and normal ovarian function in females.

Abeliovich D, Dagan J, Kimchi-Sarfaty C, Zlotogora J. Abeliovich D, et al. Am J Med Genet. 1995 Jan 30;55(3):359-62. doi: 10.1002/ajmg.1320550322. Am J Med Genet. 1995. PMID: 7726237

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: 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

4

Combined enzymatic and linkage analysis for heterozygote detection in Hunter syndrome: identification of an apparent case of germinal mosaicism.

Ben Simon-Schiff E, Bach G, Zlotogora J, Abeliovich D. Ben Simon-Schiff E, et al. Among authors: abeliovich d. Am J Med Genet. 1993 Nov 1;47(6):837-42. doi: 10.1002/ajmg.1320470608. Am J Med Genet. 1993. PMID: 7904121

5

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. Among authors: abeliovich d. Am J Med Genet. 1994 Aug 1;52(1):79-84. doi: 10.1002/ajmg.1320520116. Am J Med Genet. 1994. PMID: 7977468

6

Familial café au lait spots: a variant of neurofibromatosis type 1.

Abeliovich D, Gelman-Kohan Z, Silverstein S, Lerer I, Chemke J, Merin S, Zlotogora J. Abeliovich D, et al. J Med Genet. 1995 Dec;32(12):985-6. doi: 10.1136/jmg.32.12.985. J Med Genet. 1995. PMID: 8825931 Free PMC article.

7

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.

8

Simultaneous formation of inv dup(15) and dup(15q) in a girl with developmental delay: origin of the abnormal chromosomes.

Abeliovich D, Dagan J, Werner M, Lerer I, Shapira Y, Meiner V. Abeliovich D, et al. Eur J Hum Genet. 1995;3(1):49-55. doi: 10.1159/000472273. Eur J Hum Genet. 1995. PMID: 7767656

9

Myotonic dystrophy: molecular analysis of Israeli patients.

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

10

Isochromosome 18p in a mother and her child.

Abeliovich D, Dagan J, Levy A, Steinberg A, Zlotogora J. Abeliovich D, et al. Am J Med Genet. 1993 Jun 1;46(4):392-3. doi: 10.1002/ajmg.1320460409. Am J Med Genet. 1993. PMID: 8357009

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