Hansson KB - Search Results

1

X-chromosome duplications in males with mental retardation: pathogenic or benign variants?

Gijsbers AC, den Hollander NS, Helderman-van de Enden AT, Schuurs-Hoeijmakers JH, Vijfhuizen L, Bijlsma EK, van Haeringen A, Hansson KB, Bakker E, Breuning MH, Ruivenkamp CA. Gijsbers AC, et al. Among authors: hansson kb. Clin Genet. 2011 Jan;79(1):71-8. doi: 10.1111/j.1399-0004.2010.01438.x. Clin Genet. 2011. PMID: 20486941

2

A complex chromosome 7q rearrangement identified in a patient with mental retardation, anxiety disorder, and autistic features.

Dauwerse JG, Ruivenkamp CA, Hansson K, Marijnissen GM, Peters DJ, Breuning MH, Hilhorst-Hofstee Y. Dauwerse JG, et al. Am J Med Genet A. 2010 Feb;152A(2):427-33. doi: 10.1002/ajmg.a.33203. Am J Med Genet A. 2010. PMID: 20082467

3

Additional cryptic CNVs in mentally retarded patients with apparently balanced karyotypes.

Gijsbers AC, Bosch CA, Dauwerse JG, Giromus O, Hansson K, Hilhorst-Hofstee Y, Kriek M, van Haeringen A, Bijlsma EK, Bakker E, Breuning MH, Ruivenkamp CA. Gijsbers AC, et al. Eur J Med Genet. 2010 Sep-Oct;53(5):227-33. doi: 10.1016/j.ejmg.2010.06.003. Epub 2010 Jun 11. Eur J Med Genet. 2010. PMID: 20542150

4

Molecular and clinical characterization of patients with a ring chromosome 11.

Hansson KB, Gijsbers AC, Oostdijk W, Rehbock JJ, de Snoo F, Ruivenkamp CA, Kant SG. Hansson KB, et al. Eur J Med Genet. 2012 Dec;55(12):708-14. doi: 10.1016/j.ejmg.2012.08.004. Epub 2012 Aug 23. Eur J Med Genet. 2012. PMID: 22975011

5

A subtle familial translocation t(3;21)(p26.3;q22.3): an apparently healthy boy with a 3p deletion and 21q duplication.

Gijsbers AC, van Haeringen A, Bosch CA, Hansson K, Verschuren M, Bakker E, Breuning MH, Ruivenkamp CA. Gijsbers AC, et al. Cytogenet Genome Res. 2010 Jun;128(4):245-9. doi: 10.1159/000302497. Epub 2010 Apr 30. Cytogenet Genome Res. 2010. PMID: 20431279

6

Clinical and molecular characterization of an infant with a tandem duplication and deletion of 19p13.

Tan RN, Witlox RS, Hilhorst-Hofstee Y, Peeters-Scholte CM, den Hollander NS, Ruivenkamp CA, Hoffer MJ, Hansson KB, van Roosmalen MJ, Kloosterman WP, Santen GW. Tan RN, et al. Among authors: hansson kb. Am J Med Genet A. 2015 Aug;167A(8):1884-9. doi: 10.1002/ajmg.a.37076. Epub 2015 Apr 21. Am J Med Genet A. 2015. PMID: 25900458

7

Interstitial deletion of 6q without phenotypic effect.

Hansson K, Szuhai K, Knijnenburg J, van Haeringen A, de Pater J. Hansson K, et al. Am J Med Genet A. 2007 Jun 15;143A(12):1354-7. doi: 10.1002/ajmg.a.31783. Am J Med Genet A. 2007. PMID: 17506100

8

Interstitial duplication in the proximal long arm of chromosome 16.

Hansson K, Dauwerse H, Gijsbers A, van Diepen M, Ruivenkamp C, Kant S. Hansson K, et al. Am J Med Genet A. 2010 Jul;152A(7):1858-61. doi: 10.1002/ajmg.a.33434. Am J Med Genet A. 2010. PMID: 20583185 No abstract available.

9

Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion.

Knijnenburg J, van Haeringen A, Hansson KB, Lankester A, Smit MJ, Belfroid RD, Bakker E, Rosenberg C, Tanke HJ, Szuhai K. Knijnenburg J, et al. Among authors: hansson kb. Eur J Hum Genet. 2007 May;15(5):548-55. doi: 10.1038/sj.ejhg.5201807. Epub 2007 Mar 7. Eur J Hum Genet. 2007. PMID: 17342151

10

Genomic imbalances in mental retardation.

Kriek M, White SJ, Bouma MC, Dauwerse HG, Hansson KB, Nijhuis JV, Bakker B, van Ommen GJ, den Dunnen JT, Breuning MH. Kriek M, et al. Among authors: hansson kb. J Med Genet. 2004 Apr;41(4):249-55. doi: 10.1136/jmg.2003.014308. J Med Genet. 2004. PMID: 15060096 Free PMC article.

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