188 related articles for article (PubMed ID: 11344308)
1. Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South Africa.
Tipping AJ; Pearson T; Morgan NV; Gibson RA; Kuyt LP; Havenga C; Gluckman E; Joenje H; de Ravel T; Jansen S; Mathew CG
Proc Natl Acad Sci U S A; 2001 May; 98(10):5734-9. PubMed ID: 11344308
[TBL] [Abstract][Full Text] [Related]
2. Founder haplotype analysis of Fanconi anemia in the Korean population finds common ancestral haplotypes for a FANCG variant.
Park J; Kim M; Jang W; Chae H; Kim Y; Chung NG; Lee JW; Cho B; Jeong DC; Park IY; Park MS
Ann Hum Genet; 2015 May; 79(3):153-61. PubMed ID: 25703136
[TBL] [Abstract][Full Text] [Related]
3. Fanconi anemia founder mutation in Macedonian patients.
Madjunkova S; Kocheva SA; Plaseska-Karanfilska D
Acta Haematol; 2014; 132(1):15-21. PubMed ID: 24356203
[TBL] [Abstract][Full Text] [Related]
4. Evidence for a founder effect for pseudoxanthoma elasticum in the Afrikaner population of South Africa.
Le Saux O; Beck K; Sachsinger C; Treiber C; Göring HH; Curry K; Johnson EW; Bercovitch L; Marais AS; Terry SF; Viljoen DL; Boyd CD
Hum Genet; 2002 Oct; 111(4-5):331-8. PubMed ID: 12384774
[TBL] [Abstract][Full Text] [Related]
5. A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain.
Callén E; Casado JA; Tischkowitz MD; Bueren JA; Creus A; Marcos R; Dasí A; Estella JM; Muñoz A; Ortega JJ; de Winter J; Joenje H; Schindler D; Hanenberg H; Hodgson SV; Mathew CG; Surrallés J
Blood; 2005 Mar; 105(5):1946-9. PubMed ID: 15522956
[TBL] [Abstract][Full Text] [Related]
6. Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations.
Bouchlaka C; Abdelhak S; Amouri A; Ben Abid H; Hadiji S; Frikha M; Ben Othman T; Amri F; Ayadi H; Hachicha M; Rebaï A; Saad A; Dellagi K;
J Hum Genet; 2003; 48(7):352-61. PubMed ID: 12827451
[TBL] [Abstract][Full Text] [Related]
7. Origin and migration of an Afrikaner founder mutation FHAfrikaner-2 (V408M) causing familial hypercholesterolemia.
Defesche JC; Van Diermen DE; Hayden MR; Kastelein JP
Gene Geogr; 1996 Apr; 10(1):1-10. PubMed ID: 8913716
[TBL] [Abstract][Full Text] [Related]
8. Identification of a common founder couple for 40 South African Afrikaner families with Parkinson's disease.
Geldenhuys G; Glanzmann B; Lombard D; Boolay S; Carr J; Bardien S
S Afr Med J; 2014 May; 104(6):413-9. PubMed ID: 25214250
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. A common Fanconi anemia mutation in black populations of sub-Saharan Africa.
Morgan NV; Essop F; Demuth I; de Ravel T; Jansen S; Tischkowitz M; Lewis CM; Wainwright L; Poole J; Joenje H; Digweed M; Krause A; Mathew CG
Blood; 2005 May; 105(9):3542-4. PubMed ID: 15657175
[TBL] [Abstract][Full Text] [Related]
11. Molecular characterization of three novel Fanconi anemia mutations in Israeli Arabs.
Tamary H; Dgany O; Toledano H; Shalev Z; Krasnov T; Shalmon L; Schechter T; Bercovich D; Attias D; Laor R; Koren A; Yaniv I
Eur J Haematol; 2004 May; 72(5):330-5. PubMed ID: 15059067
[TBL] [Abstract][Full Text] [Related]
12. Two common founder mutations of the fanconi anemia group G gene FANCG/XRCC9 in the Japanese population.
Yagasaki H; Oda T; Adachi D; Nakajima T; Nakahata T; Asano S; Yamashita T
Hum Mutat; 2003 May; 21(5):555. PubMed ID: 12673805
[TBL] [Abstract][Full Text] [Related]
13. Novel Founder Mutation in
Dimishkovska M; Kotori VM; Gucev Z; Kocheva S; Polenakovic M; Plaseska-Karanfilska D
Balkan Med J; 2018 Jan; 35(1):108-111. PubMed ID: 29400309
[TBL] [Abstract][Full Text] [Related]
14. Comprehensive analysis of pathogenic deletion variants in Fanconi anemia genes.
Flynn EK; Kamat A; Lach FP; Donovan FX; Kimble DC; Narisu N; Sanborn E; Boulad F; Davies SM; Gillio AP; Harris RE; MacMillan ML; Wagner JE; Smogorzewska A; Auerbach AD; Ostrander EA; Chandrasekharappa SC
Hum Mutat; 2014 Nov; 35(11):1342-53. PubMed ID: 25168418
[TBL] [Abstract][Full Text] [Related]
15. Quantitative PCR analysis reveals a high incidence of large intragenic deletions in the FANCA gene in Spanish Fanconi anemia patients.
Callén E; Tischkowitz MD; Creus A; Marcos R; Bueren JA; Casado JA; Mathew CG; Surrallés J
Cytogenet Genome Res; 2004; 104(1-4):341-5. PubMed ID: 15162062
[TBL] [Abstract][Full Text] [Related]
16. High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis.
Amouri A; Talmoudi F; Messaoud O; d'Enghien CD; Rekaya MB; Allegui I; Azaiez H; Kefi R; Abdelhak A; Meseddi SH; Torjemane L; Ouederni M; Mellouli F; Abid HB; Aissaoui L; Bejaoui M; Othmen TB; Lyonnet DS; Soulier J; Hachicha M; Dellagi K; Abdelhak S; Fanconi T
Mol Genet Genomic Med; 2014 Mar; 2(2):160-5. PubMed ID: 24689079
[TBL] [Abstract][Full Text] [Related]
17. The FANCA gene in Japanese Fanconi anemia: reports of eight novel mutations and analysis of sequence variability.
Tachibana A; Kato T; Ejima Y; Yamada T; Shimizu T; Yang L; Tsunematsu Y; Sasaki MS
Hum Mutat; 1999; 13(3):237-44. PubMed ID: 10090479
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. A founder BRCA2 mutation in non-Afrikaner breast cancer patients of the Western Cape of South Africa.
van der Merwe NC; Hamel N; Schneider SR; Apffelstaedt JP; Wijnen JT; Foulkes WD
Clin Genet; 2012 Feb; 81(2):179-84. PubMed ID: 21204799
[TBL] [Abstract][Full Text] [Related]
20. High frequency of large intragenic deletions in the Fanconi anemia group A gene.
Morgan NV; Tipping AJ; Joenje H; Mathew CG
Am J Hum Genet; 1999 Nov; 65(5):1330-41. PubMed ID: 10521298
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
