Search Results - Snetselaar, Reinier
- Showing 1 - 6 results of 6
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The frequency of SMN gene variants lacking exon 7 and 8 is highly population dependent by Vijzelaar, Raymon, Snetselaar, Reinier, Clausen, Martijn, Mason, Amanda G., Rinsma, Marrit, Zegers, Marinka, Molleman, Naomi, Boschloo, Renske, Yilmaz, Rizkat, Kuilboer, Romy, Lens, Sylvia, Sulchan, Syamiroh, Schouten, Jan
Published 2019Text -
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Validation of a Fast, Robust, Inexpensive, Two-Tiered Neonatal Screening Test algorithm on Dried Blood Spots for Spinal Muscular Atrophy by Strunk, Annuska, Abbes, Andre, Stuitje, Antoine R., Hettinga, Chris, Sepers, Eline M., Snetselaar, Reinier, Schouten, Jan, Asselman, Fay-Lynn, Cuppen, Inge, Lemmink, Henny, van der Pol, W. Ludo, Engel, Henk
Published 2019Text -
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Short telomere length in IPF lung associates with fibrotic lesions and predicts survival by Snetselaar, Reinier, van Batenburg, Aernoud A., van Oosterhout, Matthijs F. M., Kazemier, Karin M., Roothaan, Suzan M., Peeters, Ton, van der Vis, Joanne J., Goldschmeding, Roel, Grutters, Jan C., van Moorsel, Coline H. M.
Published 2017Text -
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SMN1 Duplications Are Associated With Progressive Muscular Atrophy, but Not With Multifocal Motor Neuropathy and Primary Lateral Sclerosis by Bos, Jeroen W., Groen, Ewout J.N., Wadman, Renske I., Curial, Chantall A.D., Molleman, Naomi N., Zegers, Marinka, van Vught, Paul W.J., Snetselaar, Reinier, Vijzelaar, Raymon, van der Pol, W. Ludo, van den Berg, Leonard H.
Published 2021Text