Chromosomal abnormalities in hepatic cysts point to novel polycystic liver disease genes

Edgar S. Wills; Wybrich R. Cnossen; Joris A. Veltman; Rob Woestenenk; Marloes Steehouwer; Jody Salomon; Rene H. M. te Morsche; Meritxell Huch; Jayne Y. Hehir-Kwa; Martijn J. Banning; Rolph Pfundt; Ronald Roepman; Alexander Hoischen; Joost P. H. Drenth

doi:10.1038/ejhg.2016.97

Chromosomal abnormalities in hepatic cysts point to novel polycystic liver disease genes

Edgar S. Wills, Wybrich R. Cnossen, Joris A. Veltman, Rob Woestenenk, Marloes Steehouwer, Jody Salomon, Rene H. M. te Morsche, Meritxell Huch, Jayne Y. Hehir-Kwa, Martijn J. Banning, Rolph Pfundt, Ronald Roepman, Alexander Hoischen, Joost P. H. Drenth

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

Original language	English
Pages (from-to)	1707-1714
Journal	European Journal of Human Genetics
Volume	24
Issue number	12
DOIs	https://doi.org/10.1038/ejhg.2016.97
Publication status	Published - Dec 2016

Cite this

Wills, E. S., Cnossen, W. R., Veltman, J. A., Woestenenk, R., Steehouwer, M., Salomon, J., te Morsche, R. H. M., Huch, M., Hehir-Kwa, J. Y., Banning, M. J., Pfundt, R., Roepman, R., Hoischen, A., & Drenth, J. P. H. (2016). Chromosomal abnormalities in hepatic cysts point to novel polycystic liver disease genes. European Journal of Human Genetics, 24(12), 1707-1714. https://doi.org/10.1038/ejhg.2016.97

Wills, Edgar S. ; Cnossen, Wybrich R. ; Veltman, Joris A. ; Woestenenk, Rob ; Steehouwer, Marloes ; Salomon, Jody ; te Morsche, Rene H. M. ; Huch, Meritxell ; Hehir-Kwa, Jayne Y. ; Banning, Martijn J. ; Pfundt, Rolph ; Roepman, Ronald ; Hoischen, Alexander ; Drenth, Joost P. H. / Chromosomal abnormalities in hepatic cysts point to novel polycystic liver disease genes. In: European Journal of Human Genetics. 2016 ; Vol. 24, No. 12. pp. 1707-1714.

@article{cd17b41bcc48491e800888b478e5464e,

title = "Chromosomal abnormalities in hepatic cysts point to novel polycystic liver disease genes",

author = "Wills, {Edgar S.} and Cnossen, {Wybrich R.} and Veltman, {Joris A.} and Rob Woestenenk and Marloes Steehouwer and Jody Salomon and {te Morsche}, {Rene H. M.} and Meritxell Huch and Hehir-Kwa, {Jayne Y.} and Banning, {Martijn J.} and Rolph Pfundt and Ronald Roepman and Alexander Hoischen and Drenth, {Joost P. H.}",

year = "2016",

month = dec,

doi = "10.1038/ejhg.2016.97",

language = "English",

volume = "24",

pages = "1707--1714",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Nature Publishing Group",

number = "12",

}

Wills, ES, Cnossen, WR, Veltman, JA, Woestenenk, R, Steehouwer, M, Salomon, J, te Morsche, RHM, Huch, M, Hehir-Kwa, JY, Banning, MJ, Pfundt, R, Roepman, R, Hoischen, A & Drenth, JPH 2016, 'Chromosomal abnormalities in hepatic cysts point to novel polycystic liver disease genes', European Journal of Human Genetics, vol. 24, no. 12, pp. 1707-1714. https://doi.org/10.1038/ejhg.2016.97

Chromosomal abnormalities in hepatic cysts point to novel polycystic liver disease genes. / Wills, Edgar S.; Cnossen, Wybrich R.; Veltman, Joris A.; Woestenenk, Rob; Steehouwer, Marloes; Salomon, Jody; te Morsche, Rene H. M.; Huch, Meritxell; Hehir-Kwa, Jayne Y.; Banning, Martijn J.; Pfundt, Rolph; Roepman, Ronald; Hoischen, Alexander; Drenth, Joost P. H.

In: European Journal of Human Genetics, Vol. 24, No. 12, 12.2016, p. 1707-1714.

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

TY - JOUR

T1 - Chromosomal abnormalities in hepatic cysts point to novel polycystic liver disease genes

AU - Wills, Edgar S.

AU - Cnossen, Wybrich R.

AU - Veltman, Joris A.

AU - Woestenenk, Rob

AU - Steehouwer, Marloes

AU - Salomon, Jody

AU - te Morsche, Rene H. M.

AU - Huch, Meritxell

AU - Hehir-Kwa, Jayne Y.

AU - Banning, Martijn J.

AU - Pfundt, Rolph

AU - Roepman, Ronald

AU - Hoischen, Alexander

AU - Drenth, Joost P. H.

PY - 2016/12

Y1 - 2016/12

U2 - 10.1038/ejhg.2016.97

DO - 10.1038/ejhg.2016.97

M3 - Article

VL - 24

SP - 1707

EP - 1714

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

SN - 1018-4813

IS - 12

ER -

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10.1038/ejhg.2016.97