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Structural analysis of a missense mutation (Val414Phe) in the catalytic core domain of the factor XIII(A) subunit.
Aslam S, Yee VC, Narayanan S, Duraisamy G, Standen GR. Aslam S, et al. Among authors: standen gr. Br J Haematol. 1997 Aug;98(2):346-52. doi: 10.1046/j.1365-2141.1997.2263043.x. Br J Haematol. 1997. PMID: 9266932
Prenatal diagnosis in factor XIII-A deficiency.
Killick CJ, Barton CJ, Aslam S, Standen G. Killick CJ, et al. Arch Dis Child Fetal Neonatal Ed. 1999 May;80(3):F238-9. doi: 10.1136/fn.80.3.f238. Arch Dis Child Fetal Neonatal Ed. 1999. PMID: 10212091 Free PMC article.
A large bruise.
Standen G, Birchall J, Morse C, Chamberlain-Webber R. Standen G, et al. Lancet. 1999 Jun 5;353(9168):1934. doi: 10.1016/S0140-6736(99)03208-0. Lancet. 1999. PMID: 10371573 No abstract available.
Optimisation and properties of a UHG for genotyping of hemoglobins S and C.
Wood N, Standen G, Old J, Bidwell J. Wood N, et al. Hum Mutat. 1995;5(2):166-72. doi: 10.1002/humu.1380050210. Hum Mutat. 1995. PMID: 7749414
Rapid mutation screening in type 2A von Willebrand's disease using universal heteroduplex generators.
Culpan D, Standen G, Wood N, Mazurier C, Gaucher C, Bidwell J. Culpan D, et al. Br J Haematol. 1997 Mar;96(3):464-9. doi: 10.1046/j.1365-2141.1997.d01-2054.x. Br J Haematol. 1997. PMID: 9054649
Rapid genotypic diagnosis of type 2A von Willebrand's disease by heteroduplex analysis.
Culpan D, Goodeve A, Bowen DJ, Standen G, Bidwell J. Culpan D, et al. Clin Lab Haematol. 1998 Jun;20(3):177-8. doi: 10.1046/j.1365-2257.1998.00111.x. Clin Lab Haematol. 1998. PMID: 9681234
Severe type III von Willebrand's disease caused by deletion of exon 42 of the von Willebrand factor gene: family studies that identify carriers of the condition and a compound heterozygous individual.
Peake IR, Liddell MB, Moodie P, Standen G, Mancuso DJ, Tuley EA, Westfield LA, Sorace JM, Sadler JE, Verweij CL, et al. Peake IR, et al. Blood. 1990 Feb 1;75(3):654-61. Blood. 1990. PMID: 2297569
Family studies and prenatal diagnosis in severe von Willebrand disease by polymerase chain reaction amplification of a variable number tandem repeat region of the von Willebrand factor gene.
Peake IR, Bowen D, Bignell P, Liddell MB, Sadler JE, Standen G, Bloom AL. Peake IR, et al. Blood. 1990 Aug 1;76(3):555-61. Blood. 1990. PMID: 2378985
RT-PCR permits simultaneous genotyping of thiopurine S-methyltransferase allelic variants by multiplex induced heteroduplex analysis.
Wood N, Fraser A, Bidwell J, Standen G. Wood N, et al. Hum Mutat. 2004 Jul;24(1):93-9. doi: 10.1002/humu.20057. Hum Mutat. 2004. PMID: 15221793
An investigation of the association of the factor V Leiden mutation and inflammatory bowel disease.
Haslam N, Standen GR, Probert CS. Haslam N, et al. Among authors: standen gr. Eur J Gastroenterol Hepatol. 1999 Nov;11(11):1289-91. doi: 10.1097/00042737-199911000-00018. Eur J Gastroenterol Hepatol. 1999. PMID: 10563542
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