158 related articles for article (PubMed ID: 10464622)
1. Fanconi anemia: genetic testing in Ashkenazi Jews.
Auerbach AD
Genet Test; 1997; 1(1):27-33. PubMed ID: 10464622
[TBL] [Abstract][Full Text] [Related]
2. Carrier frequency of the IVS4 + 4 A-->T mutation of the Fanconi anemia gene FAC in the Ashkenazi Jewish population.
Verlander PC; Kaporis A; Liu Q; Zhang Q; Seligsohn U; Auerbach AD
Blood; 1995 Dec; 86(11):4034-8. PubMed ID: 7492758
[TBL] [Abstract][Full Text] [Related]
3. The Ashkenazi Jewish Fanconi anemia mutation: incidence among patients and carrier frequency in the at-risk population.
Whitney MA; Jakobs P; Kaback M; Moses RE; Grompe M
Hum Mutat; 1994; 3(4):339-41. PubMed ID: 8081385
[TBL] [Abstract][Full Text] [Related]
4. Fanconi anemia in Ashkenazi Jews.
Kutler DI; Auerbach AD
Fam Cancer; 2004; 3(3-4):241-8. PubMed ID: 15516848
[TBL] [Abstract][Full Text] [Related]
5. The molecular biology of Fanconi anemia.
Tamary H; Bar-Yam R; Zemach M; Dgany O; Shalmon L; Yaniv I
Isr Med Assoc J; 2002 Oct; 4(10):819-23. PubMed ID: 12389351
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Spectrum of sequence variations in the FANCA gene: an International Fanconi Anemia Registry (IFAR) study.
Levran O; Diotti R; Pujara K; Batish SD; Hanenberg H; Auerbach AD
Hum Mutat; 2005 Feb; 25(2):142-9. PubMed ID: 15643609
[TBL] [Abstract][Full Text] [Related]
8. A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews.
Whitney MA; Saito H; Jakobs PM; Gibson RA; Moses RE; Grompe M
Nat Genet; 1993 Jun; 4(2):202-5. PubMed ID: 8348157
[TBL] [Abstract][Full Text] [Related]
9. Phenotypic consequences of mutations in the Fanconi anemia FAC gene: an International Fanconi Anemia Registry study.
Gillio AP; Verlander PC; Batish SD; Giampietro PF; Auerbach AD
Blood; 1997 Jul; 90(1):105-10. PubMed ID: 9207444
[TBL] [Abstract][Full Text] [Related]
10. The IVS4 + 4 A to T mutation of the fanconi anemia gene FANCC is not associated with a severe phenotype in Japanese patients.
Futaki M; Yamashita T; Yagasaki H; Toda T; Yabe M; Kato S; Asano S; Nakahata T
Blood; 2000 Feb; 95(4):1493-8. PubMed ID: 10666230
[TBL] [Abstract][Full Text] [Related]
11. [Fanconi anemia: cytogenetic diagnosis of 40 cases].
Porto B; Sousa R; Ponte F; Torgal A; Campilho F; Campos A; Gonçalves C; Barbot J
Acta Med Port; 2011; 24(3):405-12. PubMed ID: 22015027
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Fanconi anaemia group A (FANCA) mutations in Israeli non-Ashkenazi Jewish patients.
Tamary H; Bar-Yam R; Shalmon L; Rachavi G; Krostichevsky M; Elhasid R; Barak Y; Kapelushnik J; Yaniv I; Auerbach AD; Zaizov R
Br J Haematol; 2000 Oct; 111(1):338-43. PubMed ID: 11091222
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutations.
Dokal I; Chase A; Morgan NV; Coulthard S; Hall G; Mathew CG; Roberts I
Br J Haematol; 1996 Jun; 93(4):813-6. PubMed ID: 8703809
[TBL] [Abstract][Full Text] [Related]
16. Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3.
Pronk JC; Gibson RA; Savoia A; Wijker M; Morgan NV; Melchionda S; Ford D; Temtamy S; Ortega JJ; Jansen S
Nat Genet; 1995 Nov; 11(3):338-40. PubMed ID: 7581462
[TBL] [Abstract][Full Text] [Related]
17. Positional cloning of the Fanconi anaemia group A gene.
Fanconi anaemia/Breast cancer consortium
Nat Genet; 1996 Nov; 14(3):324-8. PubMed ID: 8896564
[TBL] [Abstract][Full Text] [Related]
18. Niemann-Pick disease: mutation update, genotype/phenotype correlations, and prospects for genetic testing.
Schuchman EH; Miranda SR
Genet Test; 1997; 1(1):13-9. PubMed ID: 10464620
[TBL] [Abstract][Full Text] [Related]
19. Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.
Lo Ten Foe JR; Rooimans MA; Bosnoyan-Collins L; Alon N; Wijker M; Parker L; Lightfoot J; Carreau M; Callen DF; Savoia A; Cheng NC; van Berkel CG; Strunk MH; Gille JJ; Pals G; Kruyt FA; Pronk JC; Arwert F; Buchwald M; Joenje H
Nat Genet; 1996 Nov; 14(3):320-3. PubMed ID: 8896563
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
