Orr-Urtreger A - Search Results

1

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

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

Computer resources for the clinical and molecular geneticist.

Yaron Y, Orr-Urtreger A. Yaron Y, et al. Methods Mol Biol. 2000;132:291-9. doi: 10.1385/1-59259-192-2:291. Methods Mol Biol. 2000. PMID: 10547842 No abstract available.

6

The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population.

Sobe T, Vreugde S, Shahin H, Berlin M, Davis N, Kanaan M, Yaron Y, Orr-Urtreger A, Frydman M, Shohat M, Avraham KB. Sobe T, et al. Hum Genet. 2000 Jan;106(1):50-7. doi: 10.1007/s004390051009. Hum Genet. 2000. PMID: 10982182

7

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

8

First trimester PAPP-A in the detection of non-Down syndrome aneuploidy.

Ochshorn Y, Kupferminc MJ, Wolman I, Orr-Urtreger A, Jaffa AJ, Yaron Y. Ochshorn Y, et al. Prenat Diagn. 2001 Jul;21(7):547-9. doi: 10.1002/pd.105. Prenat Diagn. 2001. PMID: 11494288

9

Effect of fetal gender on first trimester markers and on Down syndrome screening.

Yaron Y, Wolman I, Kupferminc MJ, Ochshorn Y, Many A, Orr-Urtreger A. Yaron Y, et al. Prenat Diagn. 2001 Dec;21(12):1027-30. doi: 10.1002/pd.178. Prenat Diagn. 2001. PMID: 11746159

10

Maternal serum HCG is higher in the presence of a female fetus as early as week 3 post-fertilization.

Yaron Y, Lehavi O, Orr-Urtreger A, Gull I, Lessing JB, Amit A, Ben-Yosef D. Yaron Y, et al. Hum Reprod. 2002 Feb;17(2):485-9. doi: 10.1093/humrep/17.2.485. Hum Reprod. 2002. PMID: 11821300

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