Orr-Urtreger A - 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. Leuk Lymphoma. 2011 Apr;52(4):642-7. doi: 10.3109/10428194.2010.551571. Epub 2011 Feb 16. Leuk Lymphoma. 2011. PMID: 21323513

2

Prevalence of the I1307K APC gene variant in Israeli Jews of differing ethnic origin and risk for colorectal cancer.

Rozen P, Shomrat R, Strul H, Naiman T, Karminsky N, Legum C, Orr-Urtreger A. Rozen P, et al. Gastroenterology. 1999 Jan;116(1):54-7. doi: 10.1016/s0016-5085(99)70228-3. Gastroenterology. 1999. PMID: 9869602

3

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. Genet Test. 1998;2(4):293-6. doi: 10.1089/gte.1998.2.293. Genet Test. 1998. PMID: 10464606

4

Fetal muscle biopsy as a diagnostic tool in Duchenne muscular dystrophy.

Nevo Y, Shomrat R, Yaron Y, Orr-Urtreger A, Harel S, Legum C. Nevo Y, et al. Prenat Diagn. 1999 Oct;19(10):921-6. doi: 10.1002/(sici)1097-0223(199910)19:10<921::aid-pd660>3.0.co;2-a. Prenat Diagn. 1999. PMID: 10521816

5

The risk of fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known fragile X families.

Geva E, Yaron Y, Shomrat R, Ben-Yehuda A, Zabari S, Peretz H, Naiman T, Yeger H, Orr-Urtreger A. Geva E, et al. Genet Test. 2000;4(3):289-92. doi: 10.1089/10906570050501524. Genet Test. 2000. PMID: 11142761

6

Novel mutations in the emerin gene in Israeli families.

Nevo Y, Ahituv S, Yaron Y, Kedmi M, Shomrat R, Legum C, Orr-Urtreger A. Nevo Y, et al. Hum Mutat. 2001 Jun;17(6):522. doi: 10.1002/humu.1139. Hum Mutat. 2001. PMID: 11385714

7

Rett syndrome: clinical manifestations in males with MECP2 mutations.

Zeev BB, Yaron Y, Schanen NC, Wolf H, Brandt N, Ginot N, Shomrat R, Orr-Urtreger A. Zeev BB, et al. J Child Neurol. 2002 Jan;17(1):20-4. doi: 10.1177/088307380201700105. J Child Neurol. 2002. PMID: 11913564

8

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. Hum Mutat. 2002 Jun;19(6):664. doi: 10.1002/humu.9037. Hum Mutat. 2002. PMID: 12007223 Review.

9

Clinical and screening implications of the I1307K adenomatous polyposis coli gene variant in Israeli Ashkenazi Jews with familial colorectal neoplasia. Evidence for a founder effect.

Rozen P, Naiman T, Strul H, Taussky P, Karminsky N, Shomrat R, Samuel Z, Yaron Y, Orr-Urtreger A. Rozen P, et al. Cancer. 2002 May 15;94(10):2561-8. doi: 10.1002/cncr.10529. Cancer. 2002. PMID: 12173321 Free article.

10

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. Hum Mutat. 2002 Oct;20(4):323-4. doi: 10.1002/humu.9069. Hum Mutat. 2002. PMID: 12325033

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