Zlotogora J - Search Results

1

A novel mutation disrupting the cytoplasmic domain of CRB1 in a large consanguineous family of Palestinian origin affected with Leber congenital amaurosis.

Gerber S, Perrault I, Hanein S, Shalev S, Zlotogora J, Barbet F, Ducroq D, Dufier J, Munnich A, Rozet J, Kaplan J. Gerber S, et al. Among authors: zlotogora j. Ophthalmic Genet. 2002 Dec;23(4):225-35. doi: 10.1076/opge.23.4.225.13879. Ophthalmic Genet. 2002. PMID: 12567265

2

The consequences of consanguinity on the rates of malformations and major medical conditions at birth and in early childhood in inbred populations.

Zlotogora J, Shalev SA. Zlotogora J, et al. Am J Med Genet A. 2010 Aug;152A(8):2023-8. doi: 10.1002/ajmg.a.33537. Am J Med Genet A. 2010. PMID: 20635393

3

Genetic disorders among Palestinian Arabs. 4: Genetic clinics in the community.

Zlotogora J, Barges S, Bisharat B, Shalev SA. Zlotogora J, et al. Am J Med Genet A. 2006 Aug 1;140(15):1644-6. doi: 10.1002/ajmg.a.31342. Am J Med Genet A. 2006. PMID: 16830330

4

Identification of a prevalent founder mutation in an Israeli Muslim Arab village confirms the role of PRCD in the aetiology of retinitis pigmentosa in humans.

Nevet MJ, Shalev SA, Zlotogora J, Mazzawi N, Ben-Yosef T. Nevet MJ, et al. Among authors: zlotogora j. J Med Genet. 2010 Aug;47(8):533-7. doi: 10.1136/jmg.2009.073619. Epub 2010 May 27. J Med Genet. 2010. PMID: 20507925

5

Genetic disorders among Palestinian Arabs: 3. Autosomal recessive disorders in a single village.

Zlotogora J, Shalev S, Habiballah H, Barjes S. Zlotogora J, et al. Am J Med Genet. 2000 Jun 19;92(5):343-5. doi: 10.1002/1096-8628(20000619)92:5<343::aid-ajmg9>3.0.co;2-i. Am J Med Genet. 2000. PMID: 10861664

6

A long-term follow up of premarital counseling in the Israeli Arab population.

Zlotogora J, Shalev SA. Zlotogora J, et al. J Community Genet. 2014 Oct;5(4):377-81. doi: 10.1007/s12687-014-0192-2. Epub 2014 Jun 29. J Community Genet. 2014. PMID: 24974306 Free PMC article.

7

The fate of 12 recessive mutations in a single village.

Zlotogora J, Hujerat Y, Barges S, Shalev SA, Chakravarti A. Zlotogora J, et al. Ann Hum Genet. 2007 Mar;71(Pt 2):202-8. doi: 10.1111/j.1469-1809.2006.00308.x. Ann Hum Genet. 2007. PMID: 17331080

8

Marriage patterns and reproductive decision-making in the inhabitants of a single Muslim village during a 50-year period.

Zlotogora J, Shalev SA. Zlotogora J, et al. Hum Hered. 2014;77(1-4):10-5. doi: 10.1159/000357945. Epub 2014 Jul 29. Hum Hered. 2014. PMID: 25060265 Free article.

9

[A comprehensive program for prevention of genetic diseases among Arabs in Israel].

Shalev SA, Carmi R, Leventhal A, Zlotogora J. Shalev SA, et al. Among authors: zlotogora j. Harefuah. 2003 Nov;142(11):792-4, 804. Harefuah. 2003. PMID: 14631914 Hebrew.

10

High carriers frequency of an apparently ancient founder mutation p.Tyr322X in the ERCC8 gene responsible for Cockayne syndrome among Christian Arabs in Northern Israel.

Khayat M, Hardouf H, Zlotogora J, Shalev SA. Khayat M, et al. Among authors: zlotogora j. Am J Med Genet A. 2010 Dec;152A(12):3091-4. doi: 10.1002/ajmg.a.33746. Am J Med Genet A. 2010. PMID: 21108394

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