Hansson KB - Search Results

1

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.

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

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.

5

Tall stature and duplication of the insulin-like growth factor I receptor gene.

Kant SG, Kriek M, Walenkamp MJ, Hansson KB, van Rhijn A, Clayton-Smith J, Wit JM, Breuning MH. Kant SG, et al. Among authors: hansson kb. Eur J Med Genet. 2007 Jan-Feb;50(1):1-10. doi: 10.1016/j.ejmg.2006.03.005. Epub 2006 Sep 14. Eur J Med Genet. 2007. PMID: 17056309 Review.

6

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

7

Individuals with abnormal phenotype and normal G-banding karyotype: improvement and limitations in the diagnosis by the use of 24-colour FISH.

Bezrookove V, Hansson K, van der Burg M, van der Smagt JJ, Hilhorst-Hofstee Y, Wiegant J, Beverstock GC, Raap AK, Tanke H, Breuning MH, Rosenberg C. Bezrookove V, et al. Hum Genet. 2000 Apr;106(4):392-8. doi: 10.1007/s004390000268. Hum Genet. 2000. PMID: 10830905

8

Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents.

Rosenberg C, Knijnenburg J, Bakker E, Vianna-Morgante AM, Sloos W, Otto PA, Kriek M, Hansson K, Krepischi-Santos AC, Fiegler H, Carter NP, Bijlsma EK, van Haeringen A, Szuhai K, Tanke HJ. Rosenberg C, et al. J Med Genet. 2006 Feb;43(2):180-6. doi: 10.1136/jmg.2005.032268. Epub 2005 Jun 24. J Med Genet. 2006. PMID: 15980116 Free PMC article.

9

An XX male with the sex-determining region Y gene inserted in the long arm of chromosome 16.

Dauwerse JG, Hansson KB, Brouwers AA, Peters DJ, Breuning MH. Dauwerse JG, et al. Among authors: hansson kb. Fertil Steril. 2006 Aug;86(2):463.e1-5. doi: 10.1016/j.fertnstert.2005.12.062. Epub 2006 Jun 12. Fertil Steril. 2006. PMID: 16769064 Free article.

10

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

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