Shohat M - Search Results

1

Myotonic dystrophy--no evidence for preferential transmission of the mutated allele: a prenatal analysis.

Zunz E, Abeliovich D, Halpern GJ, Magal N, Shohat M. Zunz E, et al. Among authors: shohat m. Am J Med Genet A. 2004 May 15;127A(1):50-53. doi: 10.1002/ajmg.a.20675. Am J Med Genet A. 2004. PMID: 15103717

2

Correlation between the incidence of myotonic dystrophy in different groups in Israel and the number of CTG trinucleotide repeats in the myotonin gene.

Mor-Cohen R, Magal N, Gadoth N, Shohat T, Shohat M. Mor-Cohen R, et al. Among authors: shohat t, shohat m. Am J Med Genet. 1997 Aug 8;71(2):156-9. doi: 10.1002/(sici)1096-8628(19970808)71:2<156::aid-ajmg7>3.0.co;2-w. Am J Med Genet. 1997. PMID: 9217214

3

Increased transmission of intermediate alleles of the FMR1 gene compared with normal alleles among female heterozygotes.

Drasinover V, Ehrlich S, Magal N, Taub E, Libman V, Shohat T, Halpern GJ, Shohat M. Drasinover V, et al. Among authors: shohat t, shohat m. Am J Med Genet. 2000 Jul 17;93(2):155-7. doi: 10.1002/1096-8628(20000717)93:2<155::aid-ajmg13>3.0.co;2-g. Am J Med Genet. 2000. PMID: 10869119

4

Genetic screening for autosomal recessive nonsyndromic mental retardation in an isolated population in Israel.

Basel-Vanagaite L, Taub E, Halpern GJ, Drasinover V, Magal N, Davidov B, Zlotogora J, Shohat M. Basel-Vanagaite L, et al. Among authors: shohat m. Eur J Hum Genet. 2007 Feb;15(2):250-3. doi: 10.1038/sj.ejhg.5201750. Epub 2006 Dec 6. Eur J Hum Genet. 2007. PMID: 17149387

5

Familial Mediterranean fever--a review.

Shohat M, Halpern GJ. Shohat M, et al. Genet Med. 2011 Jun;13(6):487-98. doi: 10.1097/GIM.0b013e3182060456. Genet Med. 2011. PMID: 21358337 Free article. Review.

6

Myotonic dystrophy gene analysis in affected Israeli families.

Achiron A, Magal N, Shem-Tov N, Noy S, Shohat M, Gadoth N. Achiron A, et al. Among authors: shohat m. Isr J Med Sci. 1994 Aug;30(8):622-5. Isr J Med Sci. 1994. PMID: 8045745

7

The lower incidence of myotonic dystrophy in Ashkenazic Jews compared to North African Jews is associated with a significantly lower number of CTG trinucleotide repeats.

Mor-Cohen R, Magal N, Gadoth N, Achiron A, Shohat T, Shohat M. Mor-Cohen R, et al. Among authors: shohat t, shohat m. Isr J Med Sci. 1997 Mar;33(3):190-3. Isr J Med Sci. 1997. PMID: 9313789

8

Further delineation of cerebro-osteo-nephrosis syndrome.

Udler Y, Halpern GJ, Sher C, Davidovitz M, Shohat M. Udler Y, et al. Among authors: shohat m. Am J Med Genet. 1997 Nov 12;72(4):383-5. Am J Med Genet. 1997. PMID: 9375716

9

Abnormal liver test results in myotonic dystrophy.

Achiron A, Barak Y, Magal N, Shohat M, Cohen M, Barar R, Gadoth N. Achiron A, et al. Among authors: shohat m. J Clin Gastroenterol. 1998 Jun;26(4):292-5. doi: 10.1097/00004836-199806000-00016. J Clin Gastroenterol. 1998. PMID: 9649014

10

Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) in siblings.

Senecky Y, Halpern GJ, Inbar D, Attias J, Shohat M. Senecky Y, et al. Among authors: shohat m. Am J Med Genet. 2001 Jul 1;101(3):195-7. doi: 10.1002/ajmg.1361. Am J Med Genet. 2001. PMID: 11424132 Review.

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