Publications by authors named "Margriet van Kogelenberg"

11Publications

A new acro-osteolysis syndrome caused by duplications including PTHLH.

J Hum Genet 2014 Sep 10;59(9):484-7. Epub 2014 Jul 10.

Department of Genetics, The Hospital for Sick Children, London, UK.

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http://dx.doi.org/10.1038/jhg.2014.58DOI Listing
September 2014

A novel Xp22.11 deletion causing a syndrome of craniosynostosis and periventricular nodular heterotopia.

Am J Med Genet A 2011 Dec 3;155A(12):3144-7. Epub 2011 Nov 3.

Department of Paediatrics and Child Health, Dunedin School of Medicine, Otago University, Dunedin, New Zealand.

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http://doi.wiley.com/10.1002/ajmg.a.34311
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http://dx.doi.org/10.1002/ajmg.a.34311DOI Listing
December 2011

Identification, developmental expression and regulation of the Xenopus ortholog of human FANCG/XRCC9.

Genes Cells 2007 Jul;12(7):841-51

Division of Biochemistry and Molecular Biology, Oregon Health and Science University, Portland, OR, USA.

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http://dx.doi.org/10.1111/j.1365-2443.2007.01096.xDOI Listing
July 2007