PRRT2-related phenotypes in patients with a 16p11.2 deletion

DRM Vlaskamp; PMC Callenbach; P Rump; LAA Giannini; EH Brilstra; T Dijkhuizen; YJ Vos; AMF van der Kevie-Kersemaekers; Jeroen Knijnenburg; N de Leeuw; Rick van Minkelen; CAL Ruivenkamp; APA Stegmann; OF Brouwer; CMA van Ravenswaaij-Arts

doi:10.1016/j.ejmg.2018.08.002

PRRT2-related phenotypes in patients with a 16p11.2 deletion

DRM Vlaskamp, PMC Callenbach, P Rump, LAA Giannini, EH Brilstra, T Dijkhuizen, YJ Vos, AMF van der Kevie-Kersemaekers, Jeroen Knijnenburg, N de Leeuw, Rick van Minkelen, CAL Ruivenkamp, APA Stegmann, OF Brouwer, CMA van Ravenswaaij-Arts

Clinical Genetics

Research output: Contribution to journal › Article › Academic › peer-review

31 Citations (Scopus)

18 Downloads (Pure)

Original language	Undefined/Unknown
Pages (from-to)	265-269
Number of pages	5
Journal	European Journal of Medical Genetics
Volume	62
Issue number	4
DOIs	https://doi.org/10.1016/j.ejmg.2018.08.002
Publication status	Published - 2019

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EMC OR-01

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10.1016/j.ejmg.2018.08.002

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http://hdl.handle.net/1765/109989

Cite this

Vlaskamp, DRM., Callenbach, PMC., Rump, P., Giannini, LAA., Brilstra, EH., Dijkhuizen, T., Vos, YJ., van der Kevie-Kersemaekers, AMF., Knijnenburg, J., de Leeuw, N., van Minkelen, R., Ruivenkamp, CAL., Stegmann, APA., Brouwer, OF., & van Ravenswaaij-Arts, CMA. (2019). PRRT2-related phenotypes in patients with a 16p11.2 deletion. European Journal of Medical Genetics, 62(4), 265-269. https://doi.org/10.1016/j.ejmg.2018.08.002

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title = "PRRT2-related phenotypes in patients with a 16p11.2 deletion",

author = "DRM Vlaskamp and PMC Callenbach and P Rump and LAA Giannini and EH Brilstra and T Dijkhuizen and YJ Vos and {van der Kevie-Kersemaekers}, AMF and Jeroen Knijnenburg and {de Leeuw}, N and {van Minkelen}, Rick and CAL Ruivenkamp and APA Stegmann and OF Brouwer and {van Ravenswaaij-Arts}, CMA",

year = "2019",

doi = "10.1016/j.ejmg.2018.08.002",

language = "Undefined/Unknown",

volume = "62",

pages = "265--269",

journal = "European Journal of Medical Genetics",

issn = "1769-7212",

publisher = "Elsevier Masson",

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}

Vlaskamp, DRM, Callenbach, PMC, Rump, P, Giannini, LAA, Brilstra, EH, Dijkhuizen, T, Vos, YJ, van der Kevie-Kersemaekers, AMF, Knijnenburg, J, de Leeuw, N, van Minkelen, R, Ruivenkamp, CAL, Stegmann, APA, Brouwer, OF & van Ravenswaaij-Arts, CMA 2019, 'PRRT2-related phenotypes in patients with a 16p11.2 deletion', European Journal of Medical Genetics, vol. 62, no. 4, pp. 265-269. https://doi.org/10.1016/j.ejmg.2018.08.002

TY - JOUR

T1 - PRRT2-related phenotypes in patients with a 16p11.2 deletion

AU - Vlaskamp, DRM

AU - Callenbach, PMC

AU - Rump, P

AU - Giannini, LAA

AU - Brilstra, EH

AU - Dijkhuizen, T

AU - Vos, YJ

AU - van der Kevie-Kersemaekers, AMF

AU - Knijnenburg, Jeroen

AU - de Leeuw, N

AU - van Minkelen, Rick

AU - Ruivenkamp, CAL

AU - Stegmann, APA

AU - Brouwer, OF

AU - van Ravenswaaij-Arts, CMA

PY - 2019

Y1 - 2019

U2 - 10.1016/j.ejmg.2018.08.002

DO - 10.1016/j.ejmg.2018.08.002

M3 - Article

SN - 1769-7212

VL - 62

SP - 265

EP - 269

JO - European Journal of Medical Genetics

JF - European Journal of Medical Genetics

IS - 4

ER -