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.
102 related articles for article (PubMed ID: 7863639)
21. A de novo mutation in exon 28 of the von Willebrand factor gene in a patient with type IIA von Willebrand's disease coincides with an MboI polymorphism in the von Willebrand factor pseudogene. Pérez-Casal M; Daly M; Peake I Hum Mol Genet; 1993 Dec; 2(12):2159-61. PubMed ID: 7906590 [No Abstract] [Full Text] [Related]
22. Molecular mechanisms of Lewis antigen expression. Soejima M; Koda Y Leg Med (Tokyo); 2005 Jul; 7(4):266-9. PubMed ID: 15946883 [TBL] [Abstract][Full Text] [Related]
23. Detection of a RsaI polymorphism within the human galactokinase gene (GK2) by PCR-SSCP. Lau CC; Mok SC; Kelley A; Cramer D Hum Mol Genet; 1994 Oct; 3(10):1916. PubMed ID: 7849734 [No Abstract] [Full Text] [Related]
24. A rapid restriction site screening method for the Pro207-->Leu mutation in the lipoprotein lipase gene. Lévesque G; Julien P; Deshaies Y; Lupien PJ; Ven Murthy MR Hum Mutat; 1994; 3(4):416-7. PubMed ID: 7915934 [No Abstract] [Full Text] [Related]
25. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a new method to identify the G1528C mutation in genomic DNA showing its high frequency (approximately 90%) and identification of a new mutation (T2198C). Ijlst L; Ruiter JP; Vreijling J; Wanders RJ J Inherit Metab Dis; 1996; 19(2):165-8. PubMed ID: 8739956 [No Abstract] [Full Text] [Related]
26. Identification of the antithrombin III Kyoto mutation by restriction fragment length polymorphism analysis. Masuda H; Tsuji H; Nakagawa K; Nakahara Y; Kitamura H; Ogasahara Y; Nakagawa M Int J Hematol; 1995 Jun; 61(4):197-204. PubMed ID: 8547608 [TBL] [Abstract][Full Text] [Related]
27. PCR detection of the TaqA RFLP at the DRD2 locus. Grandy DK; Zhang Y; Civelli O Hum Mol Genet; 1993 Dec; 2(12):2197. PubMed ID: 7906592 [No Abstract] [Full Text] [Related]
28. Identification of two new single-nucleotide polymorphisms in FUT3 associated with the Lewis-null phenotype. Cooling L; Gu Y Transfusion; 2003 Dec; 43(12):1760-1. PubMed ID: 14674375 [No Abstract] [Full Text] [Related]
29. Molecular analysis of plasma alpha 1,3-fucosyltransferase deficiency and development of the methods for its genotyping. Tanaka S; Yazawa S; Noguchi K; Nishimura T; Miyanaga K; Kochibe N; Poland DC; Van Dijk W ; Matta KL Exp Clin Immunogenet; 2001; 18(1):1-12. PubMed ID: 11150848 [TBL] [Abstract][Full Text] [Related]
30. Advances in molecular genetics of alpha-2- and alpha-3/4-fucosyltransferases. Costache M; Cailleau A; Fernandez-Mateos P; Oriol R; Mollicone R Transfus Clin Biol; 1997 Jul; 4(4):367-82. PubMed ID: 9269717 [TBL] [Abstract][Full Text] [Related]
31. The APC (adenomatous polyposis coli) gene: a novel mutation in an FAP patient and a DdeI polymorphism in the 5' noncoding region. Mori T; Nagase H; Aoki T; Arakawa H; Nishihira T; Mori S; Nakamura Y Hum Mutat; 1993; 2(3):240-3. PubMed ID: 8103406 [No Abstract] [Full Text] [Related]
32. PCR amplification of the Taq I B1/B2 polymorphism at intron 5 of the dopamine beta-hydroxylase gene. Wu S; Muhleman D; Comings D Psychiatr Genet; 1997; 7(1):39-40. PubMed ID: 9264137 [No Abstract] [Full Text] [Related]
33. PvuII restriction fragment length polymorphism of lipoprotein lipase in Russians. Stepanov VA; Lemza SV Hum Hered; 1993; 43(6):388-90. PubMed ID: 7904587 [TBL] [Abstract][Full Text] [Related]
34. Rapid communication: a bovine alpha-lactalbumin gene MnlI restriction fragment length polymorphism. Mao FC J Anim Sci; 1994 Feb; 72(2):529. PubMed ID: 7908901 [No Abstract] [Full Text] [Related]
39. A TaqI polymorphism in the bovine blood coagulation factor XIII a subunit gene. Russ I; Beever JE; Lewin HA Anim Genet; 1994 Dec; 25(6):433. PubMed ID: 7695131 [No Abstract] [Full Text] [Related]
40. Analysis of the BglI restriction fragment length polymorphism in the human factor VIII gene using "virtual PCR"--a novel approach employing the polymerase chain reaction in the absence of sequence information for the locus. Bowen DJ; Hampton KK Hum Genet; 1996 Aug; 98(2):219-22. PubMed ID: 8698347 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]