Hansson K - Search Results

1

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

2

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

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

Low uptake of prenatal diagnosis after established carrier status of a balanced structural chromosome abnormality in couples with recurrent miscarriage.

Vansenne F, de Borgie CA, Korevaar JC, Franssen MT, Pajkrt E, Hansson KB, Leschot NJ, Bossuyt PM, van der Veen F, Goddijn M. Vansenne F, et al. Fertil Steril. 2010 Jun;94(1):296-300.e1-3. doi: 10.1016/j.fertnstert.2009.02.020. Epub 2009 Mar 27. Fertil Steril. 2010. PMID: 19328468 Free article.

6

The social behavioral phenotype in boys and girls with an extra X chromosome (Klinefelter syndrome and Trisomy X): a comparison with autism spectrum disorder.

van Rijn S, Stockmann L, Borghgraef M, Bruining H, van Ravenswaaij-Arts C, Govaerts L, Hansson K, Swaab H. van Rijn S, et al. Among authors: hansson k. J Autism Dev Disord. 2014 Feb;44(2):310-20. doi: 10.1007/s10803-013-1860-5. J Autism Dev Disord. 2014. PMID: 23824705

7

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

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

Cerebral white matter abnormalities in 6p25 deletion syndrome.

van der Knaap MS, Kriek M, Overweg-Plandsoen WC, Hansson KB, Madan K, Starreveld JS, Schotman-Schram P, Barkhof F, Lesnik Oberstein SA. van der Knaap MS, et al. Among authors: hansson kb. AJNR Am J Neuroradiol. 2006 Mar;27(3):586-8. AJNR Am J Neuroradiol. 2006. PMID: 16551997 Free PMC article.

10

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.

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