Brøndum-Nielsen K - Search Results

1

Cancer in patients with ataxia-telangiectasia and in their relatives in the nordic countries.

Olsen JH, Hahnemann JM, Børresen-Dale AL, Brøndum-Nielsen K, Hammarström L, Kleinerman R, Kääriäinen H, Lönnqvist T, Sankila R, Seersholm N, Tretli S, Yuen J, Boice JD Jr, Tucker M. Olsen JH, et al. J Natl Cancer Inst. 2001 Jan 17;93(2):121-7. doi: 10.1093/jnci/93.2.121. J Natl Cancer Inst. 2001. PMID: 11208881

2

Breast and other cancers in 1445 blood relatives of 75 Nordic patients with ataxia telangiectasia.

Olsen JH, Hahnemann JM, Børresen-Dale AL, Tretli S, Kleinerman R, Sankila R, Hammarström L, Robsahm TE, Kääriäinen H, Bregård A, Brøndum-Nielsen K, Yuen J, Tucker M. Olsen JH, et al. Br J Cancer. 2005 Jul 25;93(2):260-5. doi: 10.1038/sj.bjc.6602658. Br J Cancer. 2005. PMID: 15942625 Free PMC article.

3

[Genetic epidemiology and cancer].

Olsen JH, Hahnemann JM, Brøndum-Nielsen K. Olsen JH, et al. Ugeskr Laeger. 2006 Jun 12;168(24):2344-8. Ugeskr Laeger. 2006. PMID: 16822417 Danish.

4

Characterization of ATM mutations in 41 Nordic families with ataxia telangiectasia.

Laake K, Jansen L, Hahnemann JM, Brondum-Nielsen K, Lönnqvist T, Kääriäinen H, Sankila R, Lähdesmäki A, Hammarström L, Yuen J, Tretli S, Heiberg A, Olsen JH, Tucker M, Kleinerman R, Børresen-Dale AL. Laake K, et al. Hum Mutat. 2000 Sep;16(3):232-46. doi: 10.1002/1098-1004(200009)16:3<232::AID-HUMU6>3.0.CO;2-L. Hum Mutat. 2000. PMID: 10980530

5

Risk for cancer in patients with Bardet-Biedl syndrome and their relatives.

Hjortshøj TD, Grønskov K, Rosenberg T, Brøndum-Nielsen K, Olsen JH. Hjortshøj TD, et al. Am J Med Genet A. 2007 Aug 1;143A(15):1699-702. doi: 10.1002/ajmg.a.31805. Am J Med Genet A. 2007. PMID: 17587209

6

Population-based risk estimates of Wilms tumor in sporadic aniridia. A comprehensive mutation screening procedure of PAX6 identifies 80% of mutations in aniridia.

Grønskov K, Olsen JH, Sand A, Pedersen W, Carlsen N, Bak Jylling AM, Lyngbye T, Brøndum-Nielsen K, Rosenberg T. Grønskov K, et al. Hum Genet. 2001 Jul;109(1):11-8. doi: 10.1007/s004390100529. Hum Genet. 2001. PMID: 11479730

7

[There is no basis to doubt the reliability of prenatal diagnosis and counseling in Turner syndrome. Misleading registry studies].

Hahnemann JM, Brøndum-Nielsen K. Hahnemann JM, et al. Ugeskr Laeger. 1997 Oct 6;159(41):6084-6; discussion 6086-7. Ugeskr Laeger. 1997. PMID: 9381584 Danish. No abstract available.

8

[Quality assurance of chromosome examinations in the samples of amniotic fluid and placenta. A 6-year follow-up: no sign of analytic errors in 6384 samples].

Brøndum-Nielsen K, Hahnemann JM. Brøndum-Nielsen K, et al. Ugeskr Laeger. 1999 Feb 8;161(6):803-4. Ugeskr Laeger. 1999. PMID: 10028888 Danish. No abstract available.

9

No evidence for pathogenic variants or maternal effect of ZFP57 as the cause of Beckwith-Wiedemann Syndrome.

Boonen SE, Hahnemann JM, Mackay D, Tommerup N, Brøndum-Nielsen K, Tümer Z, Grønskov K. Boonen SE, et al. Eur J Hum Genet. 2012 Jan;20(1):119-21. doi: 10.1038/ejhg.2011.140. Epub 2011 Aug 24. Eur J Hum Genet. 2012. PMID: 21863059 Free PMC article.

10

Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter.

Sogaard M, Tümer Z, Hjalgrim H, Hahnemann J, Friis B, Ledaal P, Pedersen VF, Baekgaard P, Tommerup N, Cingöz S, Duno M, Brondum-Nielsen K. Sogaard M, et al. BMC Med Genet. 2005 May 17;6:21. doi: 10.1186/1471-2350-6-21. BMC Med Genet. 2005. PMID: 15904506 Free PMC article.

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