94 related articles for article (PubMed ID: 21312314)
1. Patterns of human genetic variation inferred from comparative analysis of allelic mutations in blood group antigen genes.
Patnaik SK; Blumenfeld OO
Hum Mutat; 2011 Mar; 32(3):263-71. PubMed ID: 21312314
[TBL] [Abstract][Full Text] [Related]
2. Allelic genes of blood group antigens: a source of human mutations and cSNPs documented in the Blood Group Antigen Gene Mutation Database.
Blumenfeld OO; Patnaik SK
Hum Mutat; 2004 Jan; 23(1):8-16. PubMed ID: 14695527
[TBL] [Abstract][Full Text] [Related]
3. Molecular genetics of RH and its clinical application.
Flegel WA
Transfus Clin Biol; 2006; 13(1-2):4-12. PubMed ID: 16563832
[TBL] [Abstract][Full Text] [Related]
4. Mutation databases and other online sites as a resource for transfusion medicine: history and attributes.
Blumenfeld OO
Transfus Med Rev; 2002 Apr; 16(2):103-14. PubMed ID: 11941573
[TBL] [Abstract][Full Text] [Related]
5. ABO blood group alleles and genetic recombination.
Suzuki K
Leg Med (Tokyo); 2005 Jul; 7(4):205-12. PubMed ID: 15949965
[TBL] [Abstract][Full Text] [Related]
6. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
7. [A Bw12 blood type caused by 278C>T mutation of ABO gene].
Meng QL; Gao Y; Chen M; Duan Y; Pan LZ; Yu WJ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):482-4. PubMed ID: 22875512
[TBL] [Abstract][Full Text] [Related]
8. [Analysis on FUT1 and FUT2 gene of 10 para-Bombay individuals in China].
Guo ZH; Xiang D; Zhu ZY; Wang JL; Zhang JM; Liu X; Shen W; Chen HP
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):417-21. PubMed ID: 15476160
[TBL] [Abstract][Full Text] [Related]
9. The human FOXL2 mutation database.
Beysen D; Vandesompele J; Messiaen L; De Paepe A; De Baere E
Hum Mutat; 2004 Sep; 24(3):189-93. PubMed ID: 15300845
[TBL] [Abstract][Full Text] [Related]
10. Structural basis for red cell phenotypic changes in newly identified, naturally occurring subgroup mutants of the human blood group B glycosyltransferase.
Hosseini-Maaf B; Letts JA; Persson M; Smart E; LePennec PY; Hustinx H; Zhao Z; Palcic MM; Evans SV; Chester MA; Olsson ML
Transfusion; 2007 May; 47(5):864-75. PubMed ID: 17465952
[TBL] [Abstract][Full Text] [Related]
11. Molecular biology of partial D and weak D: implications for blood bank practice.
Flegel WA; Wagner FF
Clin Lab; 2002; 48(1-2):53-9. PubMed ID: 11833677
[TBL] [Abstract][Full Text] [Related]
12. Genetic diversity of KELnull and KELel: a nationwide Austrian survey.
Körmöczi GF; Wagner T; Jungbauer C; Vadon M; Ahrens N; Moll W; Mühlbacher A; Ozgül-Gülce S; Kleinrath T; Kilga-Nogler S; Schönitzer D; Gassner C
Transfusion; 2007 Apr; 47(4):703-14. PubMed ID: 17381630
[TBL] [Abstract][Full Text] [Related]
13. Identification of a novel A1v-O1v hybrid allele with G829A mutation in a chimeric individual of AelBel phenotype.
Sun CF; Chen DP; Tseng CP; Wang WT; Liu JP
Transfusion; 2006 May; 46(5):780-9. PubMed ID: 16686846
[TBL] [Abstract][Full Text] [Related]
14. [The molecular genetics basis for ABw07 phenotype of ABO subtype].
Zhu H; Wu Y; Li X; Hong X; Xu X; Zhu F
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Dec; 25(6):678-80. PubMed ID: 19065531
[TBL] [Abstract][Full Text] [Related]
15. Gene frequencies of ABO and Rh (D) blood group alleles in a healthy infant population in Ibadan, Nigeria.
Omotade OO; Adeyemo AA; Kayode CM; Falade SL; Ikpeme S
West Afr J Med; 1999; 18(4):294-7. PubMed ID: 10734795
[TBL] [Abstract][Full Text] [Related]
16. Blood grouping discrepancies between ABO genotype and phenotype caused by O alleles.
Yazer MH; Hosseini-Maaf B; Olsson ML
Curr Opin Hematol; 2008 Nov; 15(6):618-24. PubMed ID: 18832934
[TBL] [Abstract][Full Text] [Related]
17. Weak D type 1.1 exemplifies another complexity in weak D genotyping.
Doescher A; Flegel WA; Petershofen EK; Bauerfeind U; Wagner FF
Transfusion; 2005 Oct; 45(10):1568-73. PubMed ID: 16181206
[TBL] [Abstract][Full Text] [Related]
18. Blood group typing in five Afghan populations in the North Hindu-Kush region: implications for blood transfusion practice.
Mazières S; Temory SA; Vasseur H; Gallian P; Di Cristofaro J; Chiaroni J
Transfus Med; 2013 Jun; 23(3):167-74. PubMed ID: 23578195
[TBL] [Abstract][Full Text] [Related]
19. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.
Jensen HK
Dan Med Bull; 2002 Nov; 49(4):318-45. PubMed ID: 12553167
[TBL] [Abstract][Full Text] [Related]
20. A flexible array format for large-scale, rapid blood group DNA typing.
Hashmi G; Shariff T; Seul M; Vissavajjhala P; Hue-Roye K; Charles-Pierre D; Lomas-Francis C; Chaudhuri A; Reid ME
Transfusion; 2005 May; 45(5):680-8. PubMed ID: 15847654
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
