Brøndum-Nielsen K - Search Results

1

Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families.

Vallon-Christersson J, Cayanan C, Haraldsson K, Loman N, Bergthorsson JT, Brøndum-Nielsen K, Gerdes AM, Møller P, Kristoffersson U, Olsson H, Borg A, Monteiro AN. Vallon-Christersson J, et al. Hum Mol Genet. 2001 Feb 15;10(4):353-60. doi: 10.1093/hmg/10.4.353. Hum Mol Genet. 2001. PMID: 11157798 Free PMC article.

2

Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden.

Johannsson O, Ostermeyer EA, Håkansson S, Friedman LS, Johansson U, Sellberg G, Brøndum-Nielsen K, Sele V, Olsson H, King MC, Borg A. Johannsson O, et al. Am J Hum Genet. 1996 Mar;58(3):441-50. Am J Hum Genet. 1996. PMID: 8644702 Free PMC article.

3

Breast cancer after bilateral risk-reducing mastectomy.

Skytte AB, Crüger D, Gerster M, Laenkholm AV, Lang C, Brøndum-Nielsen K, Andersen MK, Sunde L, Kølvraa S, Gerdes AM. Skytte AB, et al. Clin Genet. 2011 May;79(5):431-7. doi: 10.1111/j.1399-0004.2010.01604.x. Epub 2011 Jan 4. Clin Genet. 2011. PMID: 21199491 Clinical Trial.

4

[Genetic counselling in monogenic cancer syndromes].

Brøndum-Nielsen K, Gerdes AM. Brøndum-Nielsen K, et al. Ugeskr Laeger. 2006 Jun 12;168(24):2350-4. Ugeskr Laeger. 2006. PMID: 16822419 Danish.

5

Congenital myopathy with fiber type disproportion: a family with a chromosomal translocation t(10;17) may indicate candidate gene regions.

Gerdes AM, Petersen MB, Schrøder HD, Wulff K, Brøndum-Nielsen K. Gerdes AM, et al. Clin Genet. 1994 Jan;45(1):11-6. doi: 10.1111/j.1399-0004.1994.tb03982.x. Clin Genet. 1994. PMID: 7908614

6

[Press, ethics and genetic screening].

Gerdes AM, Brøndum-Nielsen K, Ejlertsen B. Gerdes AM, et al. Ugeskr Laeger. 2006 Oct 2;168(40):3448; author reply 3448. Ugeskr Laeger. 2006. PMID: 17039600 Danish. No abstract available.

7

Risk-reducing mastectomy and salpingo-oophorectomy in unaffected BRCA mutation carriers: uptake and timing.

Skytte AB, Gerdes AM, Andersen MK, Sunde L, Brøndum-Nielsen K, Waldstrøm M, Kølvraa S, Crüger D. Skytte AB, et al. Clin Genet. 2010 Apr;77(4):342-9. doi: 10.1111/j.1399-0004.2009.01329.x. Epub 2010 Jan 6. Clin Genet. 2010. PMID: 20059483

8

Characterization of add(1)(p36) in non-Hodgkin lymphomas by fluorescence in situ hybridization.

Bajalica S, Brøndum-Nielsen K, Sørensen AG, Pedersen NT, Kristoffersson U, Akerman M, Anderson M, Pisa P, Nordenskjöld M. Bajalica S, et al. Genes Chromosomes Cancer. 1995 May;13(1):34-9. doi: 10.1002/gcc.2870130106. Genes Chromosomes Cancer. 1995. PMID: 7541641

9

Disease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in man.

Bugge M, Bruun-Petersen G, Brøndum-Nielsen K, Friedrich U, Hansen J, Jensen G, Jensen PK, Kristoffersson U, Lundsteen C, Niebuhr E, Rasmussen KR, Rasmussen K, Tommerup N. Bugge M, et al. J Med Genet. 2000 Nov;37(11):858-65. doi: 10.1136/jmg.37.11.858. J Med Genet. 2000. PMID: 11073540 Free PMC article.

10

Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the "critical segment" towards the telomere.

Anvret M, Nordenskjöld M, Stolpe L, Johansson L, Bröndum-Nielsen K. Anvret M, et al. Hum Genet. 1991 Mar;86(5):481-3. doi: 10.1007/BF00194637. Hum Genet. 1991. PMID: 2016087

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

205 results

Search Page