These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
287 related articles for article (PubMed ID: 10464606)
1. 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 Genet Test; 1998; 2(4):293-6. PubMed ID: 10464606 [TBL] [Abstract][Full Text] [Related]
2. Carrier frequency of the Bloom syndrome blmAsh mutation in the Ashkenazi Jewish population. Li L; Eng C; Desnick RJ; German J; Ellis NA Mol Genet Metab; 1998 Aug; 64(4):286-90. PubMed ID: 9758720 [TBL] [Abstract][Full Text] [Related]
3. Ashkenazi Jewish population frequency of the Bloom syndrome gene 2281 delta 6ins7 mutation. Roa BB; Savino CV; Richards CS Genet Test; 1999; 3(2):219-21. PubMed ID: 10464671 [TBL] [Abstract][Full Text] [Related]
4. A rapid method for detecting the predominant Ashkenazi Jewish mutation in the Bloom's syndrome gene. Straughen JE; Johnson J; McLaren D; Proytcheva M; Ellis N; German J; Groden J Hum Mutat; 1998; 11(2):175-8. PubMed ID: 9482582 [TBL] [Abstract][Full Text] [Related]
5. Bloom syndrome and Fanconi's anemia: rate and ethnic origin of mutation carriers in Israel. Peleg L; Pesso R; Goldman B; Dotan K; Omer M; Friedman E; Berkenstadt M; Reznik-Wolf H; Barkai G Isr Med Assoc J; 2002 Feb; 4(2):95-7. PubMed ID: 11876000 [TBL] [Abstract][Full Text] [Related]
6. The Ashkenazic Jewish Bloom syndrome mutation blmAsh is present in non-Jewish Americans of Spanish ancestry. Ellis NA; Ciocci S; Proytcheva M; Lennon D; Groden J; German J Am J Hum Genet; 1998 Dec; 63(6):1685-93. PubMed ID: 9837821 [TBL] [Abstract][Full Text] [Related]
7. 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 Genet Test; 2003; 7(2):139-42. PubMed ID: 12885336 [TBL] [Abstract][Full Text] [Related]
8. Coinheritance of BRCA1 and BRCA2 mutations with Fanconi anemia and Bloom syndrome mutations in Ashkenazi Jewish population: possible role in risk modification for cancer development. Koren-Michowitz M; Friedman E; Gershoni-Baruch R; Brok-Simoni F; Patael Y; Rechavi G; Amariglio N Am J Hematol; 2005 Mar; 78(3):203-6. PubMed ID: 15726604 [TBL] [Abstract][Full Text] [Related]
9. Prevalence of Bloom syndrome heterozygotes among Ashkenazi Jews. Oddoux C; Clayton CM; Nelson HR; Ostrer H Am J Hum Genet; 1999 Apr; 64(4):1241-3. PubMed ID: 10090915 [No Abstract] [Full Text] [Related]
10. Prevalence of breast and colorectal cancer in Ashkenazi Jewish carriers of Fanconi anemia and Bloom syndrome. Baris HN; Kedar I; Halpern GJ; Shohat T; Magal N; Ludman MD; Shohat M Isr Med Assoc J; 2007 Dec; 9(12):847-50. PubMed ID: 18210922 [TBL] [Abstract][Full Text] [Related]
11. Relatively common mutations of the Bloom syndrome gene in the Japanese population. Kaneko H; Isogai K; Fukao T; Matsui E; Kasahara K; Yachie A; Seki H; Koizumi S; Arai M; Utunomiya J; Miki Y; Kondo N Int J Mol Med; 2004 Sep; 14(3):439-42. PubMed ID: 15289897 [TBL] [Abstract][Full Text] [Related]
12. Linkage disequilibrium between the FES, D15S127, and BLM loci in Ashkenazi Jews with Bloom syndrome. Ellis NA; Roe AM; Kozloski J; Proytcheva M; Falk C; German J Am J Hum Genet; 1994 Sep; 55(3):453-60. PubMed ID: 8079989 [TBL] [Abstract][Full Text] [Related]
13. Localization of cancer susceptibility genes by genome-wide single-nucleotide polymorphism linkage-disequilibrium mapping. Mitra N; Ye TZ; Smith A; Chuai S; Kirchhoff T; Peterlongo P; Nafa K; Phillips MS; Offit K; Ellis NA Cancer Res; 2004 Nov; 64(21):8116-25. PubMed ID: 15520224 [TBL] [Abstract][Full Text] [Related]
14. BLM heterozygosity and the risk of colorectal cancer. Gruber SB; Ellis NA; Scott KK; Almog R; Kolachana P; Bonner JD; Kirchhoff T; Tomsho LP; Nafa K; Pierce H; Low M; Satagopan J; Rennert H; Huang H; Greenson JK; Groden J; Rapaport B; Shia J; Johnson S; Gregersen PK; Harris CC; Boyd J; Rennert G; Offit K Science; 2002 Sep; 297(5589):2013. PubMed ID: 12242432 [No Abstract] [Full Text] [Related]
15. The I1307K APC polymorphism: prevalence in non-Ashkenazi Jews and evidence for a founder effect. Shtoyerman-Chen R; Friedman E; Figer A; Carmel M; Patael Y; Rath P; Fidder HH; Bar-Meir S; Theodor L Genet Test; 2001; 5(2):141-6. PubMed ID: 11551102 [TBL] [Abstract][Full Text] [Related]
16. Clinical and genetic findings in an Ashkenazi Jewish population with colorectal neoplasms. Zauber NP; Sabbath-Solitare M; Marotta S; Zauber AG; Foulkes W; Chan M; Turner F; Bishop DT Cancer; 2005 Aug; 104(4):719-29. PubMed ID: 15959913 [TBL] [Abstract][Full Text] [Related]
17. Expression of BLM (the causative gene for Bloom syndrome) and screening of Bloom syndrome. Morimoto W; Kaneko H; Isogai K; Kasahara K; Kondo N Int J Mol Med; 2002 Jul; 10(1):95-9. PubMed ID: 12060858 [TBL] [Abstract][Full Text] [Related]
18. Chromosomal instability associated with a novel BLM frameshift mutation (c.1980-1982delAA) in two unrelated Tunisian families with Bloom syndrome. Ben Salah G; Salem IH; Masmoudi A; Ben Rhouma B; Turki H; Fakhfakh F; Ayadi H; Kamoun H J Eur Acad Dermatol Venereol; 2014 Oct; 28(10):1318-23. PubMed ID: 24118499 [TBL] [Abstract][Full Text] [Related]
19. Syndrome-causing mutations of the BLM gene in persons in the Bloom's Syndrome Registry. German J; Sanz MM; Ciocci S; Ye TZ; Ellis NA Hum Mutat; 2007 Aug; 28(8):743-53. PubMed ID: 17407155 [TBL] [Abstract][Full Text] [Related]
20. The Tyr978X BRCA1 mutation: occurrence in non-Jewish Iranians and haplotype in French-Canadian and non-Ashkenazi Jews. Quintana-Murci L; Gal I; Bakhan T; Quach H; Sayar SH; Shiri-Sverdlov R; Baruch RG; McElreavey K; Dagan E; Narod S; Friedman E Fam Cancer; 2005; 4(2):85-8. PubMed ID: 15951957 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]