Christiansen M - Search Results

1

Novel feto-specific mRNA species suitable for identification of fetal cells from the maternal circulation.

Boye K, Hougaard DM, Ebbesen P, Vuust J, Christiansen M. Boye K, et al. Among authors: christiansen m. Prenat Diagn. 2001 Oct;21(10):806-12. Prenat Diagn. 2001. PMID: 11746119

2

Quantitative detection of male DNA by polymerase chain reaction using a single primer set: application to sex determination and counting of rare fetal cells.

Larsen LA, Christiansen M, Norgaard-Pedersen B, Vuust J. Larsen LA, et al. Among authors: christiansen m. Anal Biochem. 1996 Aug 15;240(1):148-50. doi: 10.1006/abio.1996.0342. Anal Biochem. 1996. PMID: 8811895 No abstract available.

3

Schwangerschaftsprotein 1 (SP1) as a maternal serum marker for Down syndrome in the first and second trimesters.

Qin QP, Christiansen M, Nguyen TH, Sørensen S, Larsen SO, Nørgaard-Pedersen B. Qin QP, et al. Among authors: christiansen m. Prenat Diagn. 1997 Feb;17(2):101-8. doi: 10.1002/(sici)1097-0223(199702)17:2<101::aid-pd4>3.0.co;2-h. Prenat Diagn. 1997. PMID: 9061756

4

Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndrome.

Kanters JK, Larsen LA, Orholm M, Agner E, Andersen PS, Vuust J, Christiansen M. Kanters JK, et al. Among authors: christiansen m. J Cardiovasc Electrophysiol. 1998 Jun;9(6):620-4. doi: 10.1111/j.1540-8167.1998.tb00944.x. J Cardiovasc Electrophysiol. 1998. PMID: 9654228

5

Inclusion of serum marker measurements from a previous pregnancy improves Down syndrome screening performance.

Larsen SO, Christiansen M, Nørgaard-Pedersen B. Larsen SO, et al. Among authors: christiansen m. Prenat Diagn. 1998 Jul;18(7):706-12. Prenat Diagn. 1998. PMID: 9706652

6

Mutation Detection by Cleavase in Combination With Capillary Electrophoresis Analysis: Application to Mutations Causing Hypertrophic Cardiomyopathy and Long-QT Syndrome.

Andersen PS, Larsen LA, Kanters Jr Jr, Havndrup O, Bundgaard H, Brandt NJ, Vuust J, Christiansen M. Andersen PS, et al. Among authors: christiansen m. Mol Diagn. 1998 Jun;3(2):105-111. doi: 10.154/MODI00300105. Mol Diagn. 1998. PMID: 10029661

7

A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome.

Larsen LA, Andersen PS, Kanters JK, Jacobsen JR, Vuust J, Christiansen M. Larsen LA, et al. Among authors: christiansen m. Clin Chim Acta. 1999 Feb;280(1-2):113-25. doi: 10.1016/s0009-8981(98)00177-6. Clin Chim Acta. 1999. PMID: 10090529

8

High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: robust multiplex analysis and pattern-based identification of allelic variants.

Larsen LA, Christiansen M, Vuust J, Andersen PS. Larsen LA, et al. Among authors: christiansen m. Hum Mutat. 1999;13(4):318-27. doi: 10.1002/(SICI)1098-1004(1999)13:4<318::AID-HUMU9>3.0.CO;2-F. Hum Mutat. 1999. PMID: 10220146

9

Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chain.

Bundgaard H, Havndrup O, Andersen PS, Larsen LA, Brandt NJ, Vuust J, Kjeldsen K, Christiansen M. Bundgaard H, et al. Among authors: christiansen m. J Mol Cell Cardiol. 1999 Apr;31(4):745-50. doi: 10.1006/jmcc.1998.0911. J Mol Cell Cardiol. 1999. PMID: 10329202

10

Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene.

Larsen LA, Fosdal I, Andersen PS, Kanters JK, Vuust J, Wettrell G, Christiansen M. Larsen LA, et al. Among authors: christiansen m. Eur J Hum Genet. 1999 Sep;7(6):724-8. doi: 10.1038/sj.ejhg.5200323. Eur J Hum Genet. 1999. PMID: 10482963

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