Gregersen N - Search Results

1

Oligonucleotide-priming methods for the chromosome-specific labelling of alpha satellite DNA in situ.

Koch JE, Kølvraa S, Petersen KB, Gregersen N, Bolund L. Koch JE, et al. Among authors: gregersen n. Chromosoma. 1989 Oct;98(4):259-65. doi: 10.1007/BF00327311. Chromosoma. 1989. PMID: 2612286

2

Alpha 1-antitrypsin alleles in patients with pulmonary emphysema, detected by DNA amplification (PCR) and oligonucleotide probes.

Bruun-Petersen K, Bruun-Petersen G, Dahl R, Larsen B, Kølvraa S, Koch J, Bolund L, Gregersen N. Bruun-Petersen K, et al. Among authors: gregersen n. Eur Respir J. 1992 May;5(5):531-7. Eur Respir J. 1992. PMID: 1612154

3

Application of fluorescence in situ hybridization techniques in clinical genetics: use of two alphoid repeat probes detecting the centromeres of chromosomes 13 and 21 or chromosomes 14 and 22, respectively.

Kølvraa S, Koch J, Gregersen N, Jensen PK, Jørgensen AL, Petersen KB, Rasmussen K, Bolund L. Kølvraa S, et al. Among authors: gregersen n. Clin Genet. 1991 Apr;39(4):278-86. doi: 10.1111/j.1399-0004.1991.tb03026.x. Clin Genet. 1991. PMID: 1829987

4

Nonradioactive, sequence-specific detection of RNA in situ by primed in situ labeling (PRINS).

Mogensen J, Kølvraa S, Hindkjaer J, Petersen S, Koch J, Nygård M, Jensen T, Gregersen N, Junker S, Bolund L. Mogensen J, et al. Among authors: gregersen n. Exp Cell Res. 1991 Sep;196(1):92-8. doi: 10.1016/0014-4827(91)90459-8. Exp Cell Res. 1991. PMID: 1879475

5

A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization.

Koch J, Kølvraa S, Hobolt N, Petersen GB, Willard HF, Waye JS, Gregersen N, Bolund L. Koch J, et al. Among authors: gregersen n. Clin Genet. 1990 Mar;37(3):216-20. doi: 10.1111/j.1399-0004.1990.tb03505.x. Clin Genet. 1990. PMID: 2323091

6

In situ hybridization analysis of isodicentric X-chromosomes with short arm fusion.

Koch JE, Kølvraa S, Hertz JM, Rasmussen K, Gregersen N, Fly GF, Bolund LA. Koch JE, et al. Among authors: gregersen n. Clin Genet. 1990 Jun;37(6):450-5. doi: 10.1111/j.1399-0004.1990.tb03529.x. Clin Genet. 1990. PMID: 2383931

7

Detection of point mutations in amplified single copy genes by biotin-labelled oligonucleotides: diagnosis of variants of alpha-1-antitrypsin.

Gregersen N, Winter V, Petersen KB, Koch J, Kølvraa S, Rüdiger N, Heinsvig EM, Bolund L. Gregersen N, et al. Clin Chim Acta. 1989 Jun 30;182(2):151-64. doi: 10.1016/0009-8981(89)90074-0. Clin Chim Acta. 1989. PMID: 2789112

8

Specific diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in dried blood spots by a polymerase chain reaction (PCR) assay detecting a point-mutation (G985) in the MCAD gene.

Gregersen N, Blakemore AI, Winter V, Andresen B, Kølvraa S, Bolund L, Curtis D, Engel PC. Gregersen N, et al. Clin Chim Acta. 1991 Nov 9;203(1):23-34. doi: 10.1016/0009-8981(91)90153-4. Clin Chim Acta. 1991. PMID: 1769118

9

Prenatal diagnosis of alpha-1-antitrypsin deficiency using polymerase chain reaction (PCR). Comparison of conventional RFLP methods with PCR used in combination with allele specific oligonucleotides or RFLP analysis.

Schwartz M, Petersen KB, Gregersen N, Hinkel K, Newton CR. Schwartz M, et al. Among authors: gregersen n. Clin Genet. 1989 Dec;36(6):419-26. Clin Genet. 1989. PMID: 2574085

10

Treatment of genomic DNA with T4 DNA ligase improves Southern blot analysis.

Koch JE, Kølvraa S, Corneliusen M, Petersen KB, Gregersen N, Bolund LA. Koch JE, et al. Among authors: gregersen n. Nucleic Acids Res. 1988 Nov 11;16(21):10387. doi: 10.1093/nar/16.21.10387. Nucleic Acids Res. 1988. PMID: 3194221 Free PMC article.

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