Shomrat R - Search Results

1

Predictive value of TP53 fluorescence in situ hybridization in cytogenetic subgroups of acute myeloid leukemia.

Tavor S, Rothman R, Golan T, Voskoboinik N, Katz BZ, Sarid N, Shomrat R, Orr-Urtreger A, Naparstek E. Tavor S, et al. Among authors: shomrat r. Leuk Lymphoma. 2011 Apr;52(4):642-7. doi: 10.3109/10428194.2010.551571. Epub 2011 Feb 16. Leuk Lymphoma. 2011. PMID: 21323513

2

Cytogenetic analysis of sinonasal carcinomas.

Gil Z, Orr-Urtreger A, Voskoboinik N, Trejo-Leider L, Spektor S, Shomrat R, Fliss DM. Gil Z, et al. Among authors: shomrat r. Otolaryngol Head Neck Surg. 2006 Apr;134(4):654-60. doi: 10.1016/j.otohns.2005.10.055. Otolaryngol Head Neck Surg. 2006. PMID: 16564392

3

Cytogenetic analysis of 101 skull base tumors.

Gil Z, Orr-Urtreger A, Voskoboinik N, Trejo-Leider L, Shomrat R, Fliss DM. Gil Z, et al. Among authors: shomrat r. Head Neck. 2008 May;30(5):567-81. doi: 10.1002/hed.20741. Head Neck. 2008. PMID: 18098307

4

Large-scale population screening for spinal muscular atrophy: clinical implications.

Ben-Shachar S, Orr-Urtreger A, Bardugo E, Shomrat R, Yaron Y. Ben-Shachar S, et al. Among authors: shomrat r. Genet Med. 2011 Feb;13(2):110-4. doi: 10.1097/GIM.0b013e3182017c05. Genet Med. 2011. PMID: 21233719 Free article.

5

MECP2 mutations in Israel: implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndrome.

Yaron Y, Ben Zeev B, Shomrat R, Bercovich D, Naiman T, Orr-Urtreger A. Yaron Y, et al. Among authors: shomrat r. Hum Mutat. 2002 Oct;20(4):323-4. doi: 10.1002/humu.9069. Hum Mutat. 2002. PMID: 12325033

6

Ethnic effect on FMR1 carrier rate and AGG repeat interruptions among Ashkenazi women.

Weiss K, Orr-Urtreger A, Kaplan Ber I, Naiman T, Shomrat R, Bardugu E, Yaron Y, Ben-Shachar S. Weiss K, et al. Among authors: shomrat r. Genet Med. 2014 Dec;16(12):940-4. doi: 10.1038/gim.2014.64. Epub 2014 May 29. Genet Med. 2014. PMID: 24875300 Free article.

7

Molecular analysis of the APC gene in 71 Israeli families: 17 novel mutations.

Gavert N, Yaron Y, Naiman T, Bercovich D, Rozen P, Shomrat R, Legum C, Orr-Urtreger A. Gavert N, et al. Among authors: shomrat r. Hum Mutat. 2002 Jun;19(6):664. doi: 10.1002/humu.9037. Hum Mutat. 2002. PMID: 12007223 Review.

8

Multiplex nested PCR for preimplantation genetic diagnosis of spinal muscular atrophy.

Malcov M, Schwartz T, Mei-Raz N, Yosef DB, Amit A, Lessing JB, Shomrat R, Orr-Urtreger A, Yaron Y. Malcov M, et al. Among authors: shomrat r. Fetal Diagn Ther. 2004 Mar-Apr;19(2):199-206. doi: 10.1159/000075151. Fetal Diagn Ther. 2004. PMID: 14764971

9

High frequency of a common Bloom syndrome Ashkenazi mutation among Jews of Polish origin.

Shahrabani-Gargir L, Shomrat R, Yaron Y, Orr-Urtreger A, Groden J, Legum C. Shahrabani-Gargir L, et al. Among authors: shomrat r. Genet Test. 1998;2(4):293-6. doi: 10.1089/gte.1998.2.293. Genet Test. 1998. PMID: 10464606

10

Screening for familial dysautonomia in Israel: evidence for higher carrier rate among Polish Ashkenazi Jews.

Lehavi O, Aizenstein O, Bercovich D, Pavzner D, Shomrat R, Orr-Urtreger A, Yaron Y. Lehavi O, et al. Among authors: shomrat r. Genet Test. 2003 Summer;7(2):139-42. doi: 10.1089/109065703322146830. Genet Test. 2003. PMID: 12885336

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