Rare novel variants in the ZIC3 gene cause X-linked heterotaxy

Aimee D. C. Paulussen; Anja Steyls; Jo Vanoevelen; Florence H. J. van Tienen; Ingrid P. C. Krapels; Godelieve R. F. Claes; Sonja Chocron; Crool Velter; Gita M. Tan-Sindhunata; Catarina Lundin; Irene Valenzuela; Balint Nagy; Iben Bache; Lisa Leth Maroun; Kristiina Avela; Han G. Brunner; Hubert J. M. Smeets; Jeroen Bakkers; Arthur van den Wijngaard

doi:10.1038/ejhg.2016.91

Rare novel variants in the ZIC3 gene cause X-linked heterotaxy

Aimee D. C. Paulussen, Anja Steyls, Jo Vanoevelen, Florence H. J. van Tienen, Ingrid P. C. Krapels, Godelieve R. F. Claes, Sonja Chocron, Crool Velter, Gita M. Tan-Sindhunata, Catarina Lundin, Irene Valenzuela, Balint Nagy, Iben Bache, Lisa Leth Maroun, Kristiina Avela, Han G. Brunner, Hubert J. M. Smeets, Jeroen Bakkers, Arthur van den Wijngaard

Clinical genetics

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

Original language	English
Pages (from-to)	1783-1791
Journal	European Journal of Human Genetics
Volume	24
Issue number	12
DOIs	https://doi.org/10.1038/ejhg.2016.91
Publication status	Published - Dec 2016

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10.1038/ejhg.2016.91

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Paulussen, A. D. C., Steyls, A., Vanoevelen, J., van Tienen, F. H. J., Krapels, I. P. C., Claes, G. R. F., ... van den Wijngaard, A. (2016). Rare novel variants in the ZIC3 gene cause X-linked heterotaxy. European Journal of Human Genetics, 24(12), 1783-1791. https://doi.org/10.1038/ejhg.2016.91

Paulussen, Aimee D. C. ; Steyls, Anja ; Vanoevelen, Jo ; van Tienen, Florence H. J. ; Krapels, Ingrid P. C. ; Claes, Godelieve R. F. ; Chocron, Sonja ; Velter, Crool ; Tan-Sindhunata, Gita M. ; Lundin, Catarina ; Valenzuela, Irene ; Nagy, Balint ; Bache, Iben ; Maroun, Lisa Leth ; Avela, Kristiina ; Brunner, Han G. ; Smeets, Hubert J. M. ; Bakkers, Jeroen ; van den Wijngaard, Arthur. / Rare novel variants in the ZIC3 gene cause X-linked heterotaxy. In: European Journal of Human Genetics. 2016 ; Vol. 24, No. 12. pp. 1783-1791.

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title = "Rare novel variants in the ZIC3 gene cause X-linked heterotaxy",

author = "Paulussen, {Aimee D. C.} and Anja Steyls and Jo Vanoevelen and {van Tienen}, {Florence H. J.} and Krapels, {Ingrid P. C.} and Claes, {Godelieve R. F.} and Sonja Chocron and Crool Velter and Tan-Sindhunata, {Gita M.} and Catarina Lundin and Irene Valenzuela and Balint Nagy and Iben Bache and Maroun, {Lisa Leth} and Kristiina Avela and Brunner, {Han G.} and Smeets, {Hubert J. M.} and Jeroen Bakkers and {van den Wijngaard}, Arthur",

year = "2016",

month = "12",

doi = "10.1038/ejhg.2016.91",

language = "English",

volume = "24",

pages = "1783--1791",

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Paulussen, ADC, Steyls, A, Vanoevelen, J, van Tienen, FHJ, Krapels, IPC, Claes, GRF, Chocron, S, Velter, C, Tan-Sindhunata, GM, Lundin, C, Valenzuela, I, Nagy, B, Bache, I, Maroun, LL, Avela, K, Brunner, HG, Smeets, HJM, Bakkers, J & van den Wijngaard, A 2016, 'Rare novel variants in the ZIC3 gene cause X-linked heterotaxy', European Journal of Human Genetics, vol. 24, no. 12, pp. 1783-1791. https://doi.org/10.1038/ejhg.2016.91

Rare novel variants in the ZIC3 gene cause X-linked heterotaxy. / Paulussen, Aimee D. C.; Steyls, Anja; Vanoevelen, Jo; van Tienen, Florence H. J.; Krapels, Ingrid P. C.; Claes, Godelieve R. F.; Chocron, Sonja; Velter, Crool; Tan-Sindhunata, Gita M.; Lundin, Catarina; Valenzuela, Irene; Nagy, Balint; Bache, Iben; Maroun, Lisa Leth; Avela, Kristiina; Brunner, Han G.; Smeets, Hubert J. M.; Bakkers, Jeroen; van den Wijngaard, Arthur.

In: European Journal of Human Genetics, Vol. 24, No. 12, 12.2016, p. 1783-1791.

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

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T1 - Rare novel variants in the ZIC3 gene cause X-linked heterotaxy

AU - Paulussen, Aimee D. C.

AU - Steyls, Anja

AU - Vanoevelen, Jo

AU - van Tienen, Florence H. J.

AU - Krapels, Ingrid P. C.

AU - Claes, Godelieve R. F.

AU - Chocron, Sonja

AU - Velter, Crool

AU - Tan-Sindhunata, Gita M.

AU - Lundin, Catarina

AU - Valenzuela, Irene

AU - Nagy, Balint

AU - Bache, Iben

AU - Maroun, Lisa Leth

AU - Avela, Kristiina

AU - Brunner, Han G.

AU - Smeets, Hubert J. M.

AU - Bakkers, Jeroen

AU - van den Wijngaard, Arthur

PY - 2016/12

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DO - 10.1038/ejhg.2016.91

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VL - 24

SP - 1783

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JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

SN - 1018-4813

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