Ten Kate LP - Search Results

1

Two families with sibling recurrence of the 17q21.31 microdeletion syndrome due to low-grade mosaicism.

Koolen DA, Dupont J, de Leeuw N, Vissers LE, van den Heuvel SP, Bradbury A, Steer J, de Brouwer AP, Ten Kate LP, Nillesen WM, de Vries BB, Parker MJ. Koolen DA, et al. Among authors: ten kate lp. Eur J Hum Genet. 2012 Jul;20(7):729-33. doi: 10.1038/ejhg.2012.1. Epub 2012 Feb 1. Eur J Hum Genet. 2012. PMID: 22293690 Free PMC article.

2

A genome-wide scan for preeclampsia in the Netherlands.

Lachmeijer AM, Arngrímsson R, Bastiaans EJ, Frigge ML, Pals G, Sigurdardóttir S, Stéfansson H, Pálsson B, Nicolae D, Kong A, Aarnoudse JG, Gulcher JR, Dekker GA, ten Kate LP, Stéfansson K. Lachmeijer AM, et al. Among authors: ten kate lp. Eur J Hum Genet. 2001 Oct;9(10):758-64. doi: 10.1038/sj.ejhg.5200706. Eur J Hum Genet. 2001. PMID: 11781687

3

Segregation ratio in cranio-cerebello-cardiac syndrome.

Stellingwerff HJ, van Hagen JM, ten Kate LP. Stellingwerff HJ, et al. Among authors: ten kate lp. Eur J Hum Genet. 2006 Sep;14(9):1054-7. doi: 10.1038/sj.ejhg.5201660. Epub 2006 May 31. Eur J Hum Genet. 2006. PMID: 16736035

4

Prenatal prediction of spinal muscular atrophy. Experience with linkage studies and consequences of present SMN deletion analysis.

Cobben JM, Scheffer H, De Visser M, Van der Steege G, Verhey JB, Osinga J, Burton M, Mensink RG, Grootscholten PM, Ten Kate LP, Buys CH. Cobben JM, et al. Among authors: ten kate lp. Eur J Hum Genet. 1996;4(4):231-6. Eur J Hum Genet. 1996. PMID: 8875190

5

Another patient with an interstitial deletion of chromosome 9: case report and a review of six cases with del(9)(q22q32).

Kroes HY, Tuerlings JH, Hordijk R, Folkers NR, ten Kate LP. Kroes HY, et al. Among authors: ten kate lp. J Med Genet. 1994 Feb;31(2):156-8. doi: 10.1136/jmg.31.2.156. J Med Genet. 1994. PMID: 8182726 Free PMC article. Review.

6

Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)].

Sijmons RH, Leegte B, van Lingen RA, de Pater JM, van der Veen AY, del Canho H, Bos C, ten Kate LP, Breed AS. Sijmons RH, et al. Among authors: ten kate lp. Am J Med Genet. 1993 Sep 15;47(4):559-62. doi: 10.1002/ajmg.1320470424. Am J Med Genet. 1993. PMID: 7504882

7

Consanguinity sans reproche.

Ten Kate LP, Scheffer H, Cornel MC, van Lookeren Campagne JG. Ten Kate LP, et al. Hum Genet. 1991 Jan;86(3):295-6. doi: 10.1007/BF00202413. Hum Genet. 1991. PMID: 1997385

8

Preconceptional ancestry-based carrier couple screening for cystic fibrosis and haemoglobinopathies: what determines the intention to participate or not and actual participation?

Lakeman P, Plass AM, Henneman L, Bezemer PD, Cornel MC, ten Kate LP. Lakeman P, et al. Among authors: ten kate lp. Eur J Hum Genet. 2009 Aug;17(8):999-1009. doi: 10.1038/ejhg.2009.1. Epub 2009 Feb 18. Eur J Hum Genet. 2009. PMID: 19223934 Free PMC article.

9

Down syndrome in the family: what to do when the karyotype of the proband is not available.

Tuerlings JH, Oosterwijk JC, ten Kate LP. Tuerlings JH, et al. Among authors: ten kate lp. Prenat Diagn. 1996 Jun;16(6):554-8. doi: 10.1002/(SICI)1097-0223(199606)16:6<554::AID-PD896>3.0.CO;2-I. Prenat Diagn. 1996. PMID: 8809898

10

Comment on Gialluisi et al.

Ten Kate LP, Teeuw M, Henneman L, Cornel MC. Ten Kate LP, et al. Eur J Hum Genet. 2014 Feb;22(2):157. doi: 10.1038/ejhg.2013.152. Epub 2013 Jul 17. Eur J Hum Genet. 2014. PMID: 23860038 Free PMC article. No abstract available.

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