Publications by authors named "Hubertus J Smeets"

6Publications

A patient with a mild holoprosencephaly spectrum phenotype and heterotaxy and a 1.3 Mb deletion encompassing GLI2.

Am J Med Genet A 2012 Jan 21;158A(1):166-73. Epub 2011 Nov 21.

Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

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http://dx.doi.org/10.1002/ajmg.a.34350DOI Listing
January 2012

Mitochondrial DNA damage analysis in bronchoalveolar lavage cells of preterm infants.

Front Biosci (Elite Ed) 2010 Jan 1;2:361-8. Epub 2010 Jan 1.

Department of Pediatrics Maastricht University Medical Center, GROW School for Oncology and Developmental Biology, 6202 AZ Maastricht, The Netherlands.

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http://dx.doi.org/10.2741/e96DOI Listing
January 2010

Influence of mutation type on clinical expression of Leber hereditary optic neuropathy.

Am J Ophthalmol 2006 Apr;141(4):676-82

Department of Genetics and Cell Biology, Maastricht University, Maastricht, The Netherlands.

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http://dx.doi.org/10.1016/j.ajo.2005.11.007DOI Listing
April 2006