Hansson K - Search Results

1

Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience.

Tuerlings JH, de France HF, Hamers A, Hordijk R, Van Hemel JO, Hansson K, Hoovers JM, Madan K, Van der Blij-Philipsen M, Gerssen-Schoorl KB, Kremer JA, Smeets DF. Tuerlings JH, et al. Among authors: hansson k. Eur J Hum Genet. 1998 May-Jun;6(3):194-200. doi: 10.1038/sj.ejhg.5200193. Eur J Hum Genet. 1998. PMID: 9781022

2

Subfertile men with constitutive chromosome abnormalities do not necessarily refrain from intracytoplasmic sperm injection treatment: a follow-up study on 75 Dutch patients.

Giltay JC, Kastrop PM, Tuerlings JH, Kremer JA, Tiemessen CH, Gerssen-Schoorl KB, van der Veen F, de Vries J, Hordijk R, Hamers GJ, Hansson K, van der Blij-Philipsen M, Govaerts LC, Pieters MH, Madan K, Scheres JM. Giltay JC, et al. Among authors: hansson k. Hum Reprod. 1999 Feb;14(2):318-20. doi: 10.1093/humrep/14.2.318. Hum Reprod. 1999. PMID: 10099971

3

Selective chromosome analysis in couples with two or more miscarriages: case-control study.

Franssen MT, Korevaar JC, Leschot NJ, Bossuyt PM, Knegt AC, Gerssen-Schoorl KB, Wouters CH, Hansson KB, Hochstenbach R, Madan K, van der Veen F, Goddijn M. Franssen MT, et al. Among authors: hansson kb. BMJ. 2005 Jul 16;331(7509):137-41. doi: 10.1136/bmj.38498.669595.8F. Epub 2005 Jun 28. BMJ. 2005. PMID: 15985440 Free PMC article.

4

[Risk factors for structural chromosomal abnormality in > or = 2 miscarriages, as an instrument for selective karyotyping].

Franssen MT, Korevaar JC, Leschot NJ, Bossuyt PM, Knegt AC, Gerssen-Schoorl KB, Wouters CH, Hansson KB, Hochstenbach PF, Madan K, van der Veen F, Goddijn M. Franssen MT, et al. Among authors: hansson kb. Ned Tijdschr Geneeskd. 2007 Apr 14;151(15):863-7. Ned Tijdschr Geneeskd. 2007. PMID: 17472118 Dutch.

5

Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD.

de Greef JC, Wohlgemuth M, Chan OA, Hansson KB, Smeets D, Frants RR, Weemaes CM, Padberg GW, van der Maarel SM. de Greef JC, et al. Among authors: hansson kb. Neurology. 2007 Sep 4;69(10):1018-26. doi: 10.1212/01.wnl.0000271391.44352.fe. Neurology. 2007. PMID: 17785671

6

Multiple genomic aberrations in a patient with mental retardation and hypogonadism: 45,X/46,X,psu dic(Y) karyotype, thyroid hormone receptor beta (THRB) mutation and heterozygosity for Wilson disease.

Hes FJ, Madan K, Rombout-Liem IS, Szuhai K, Sørensen H, van Amstel HK, Bakker E, Visser TJ, Smit JW, Hansson K. Hes FJ, et al. Among authors: hansson k. Am J Med Genet A. 2009 Oct;149A(10):2231-5. doi: 10.1002/ajmg.a.33004. Am J Med Genet A. 2009. PMID: 19725132

7

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

8

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. Among authors: hansson k. Hum Genet. 2000 Apr;106(4):392-8. doi: 10.1007/s004390000268. Hum Genet. 2000. PMID: 10830905

9

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

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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