Postzygotic telomere capture causes segmental UPD, duplication and deletion of chromosome 8p in a patient with intellectual disability and obesity

J Knijnenburg; MEW Uytdewilligen; D van Hassel; Rianne Oostenbrink; BHJ Eussen; A Klein; Alice Brooks; L van Zutven

doi:10.1016/j.ejmg.2017.06.003

Postzygotic telomere capture causes segmental UPD, duplication and deletion of chromosome 8p in a patient with intellectual disability and obesity

J Knijnenburg
, MEW Uytdewilligen
, D van Hassel
, Rianne Oostenbrink
, BHJ Eussen
, A Klein
, Alice Brooks
, L van Zutven

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

5 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	445-450
Number of pages	6
Journal	European Journal of Medical Genetics
Volume	60
Issue number	9
DOIs	https://doi.org/10.1016/j.ejmg.2017.06.003
Publication status	Published - 2017

Research programs

EMC MM-04-54-08-A

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Access to Document

10.1016/j.ejmg.2017.06.003

http://hdl.handle.net/1765/100434

Cite this

Knijnenburg, J., Uytdewilligen, MEW., van Hassel, D., Oostenbrink, R., Eussen, BHJ., Klein, A., Brooks, A., & van Zutven, L. (2017). Postzygotic telomere capture causes segmental UPD, duplication and deletion of chromosome 8p in a patient with intellectual disability and obesity. European Journal of Medical Genetics, 60(9), 445-450. https://doi.org/10.1016/j.ejmg.2017.06.003

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Knijnenburg, J, Uytdewilligen, MEW, van Hassel, D, Oostenbrink, R, Eussen, BHJ, Klein, A, Brooks, A & van Zutven, L 2017, 'Postzygotic telomere capture causes segmental UPD, duplication and deletion of chromosome 8p in a patient with intellectual disability and obesity', European Journal of Medical Genetics, vol. 60, no. 9, pp. 445-450. https://doi.org/10.1016/j.ejmg.2017.06.003

TY - JOUR

T1 - Postzygotic telomere capture causes segmental UPD, duplication and deletion of chromosome 8p in a patient with intellectual disability and obesity

AU - Knijnenburg, J

AU - Uytdewilligen, MEW

AU - van Hassel, D

AU - Oostenbrink, Rianne

AU - Eussen, BHJ

AU - Klein, A

AU - Brooks, Alice

AU - van Zutven, L

PY - 2017

Y1 - 2017

U2 - 10.1016/j.ejmg.2017.06.003

DO - 10.1016/j.ejmg.2017.06.003

M3 - Article

C2 - 28602932

SN - 1769-7212

VL - 60

SP - 445

EP - 450

JO - European Journal of Medical Genetics

JF - European Journal of Medical Genetics

IS - 9

ER -