Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19

C. Bredrup; S. Saunier; M.M. Oud; T. Fiskerstrand; A. Hoischen; D. Brackman; S.M. Leh; M. Midtbǿ; E. Filhol; C. Bole-Feysot; P. Nitschké; C. Gilissen; O.H. Haugen; J.S. Sanders; I. Stolte-Dijkstra; D.A. Mans; E.J. Steenbergen; B.C. Hamel; M. Matignon; R. Pfundt; C. Jeanpierre; H. Boman; E. Rǿdahl; J.A. Veltman; P.M. Knappskog; V.V.A.M. Knoers; R. Roepman; H.H. Arts

Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19

Translated title of the contribution: Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19

C. Bredrup, S. Saunier, M.M. Oud, T. Fiskerstrand, A. Hoischen, D. Brackman, S.M. Leh, M. Midtbǿ, E. Filhol, C. Bole-Feysot, P. Nitschké, C. Gilissen, O.H. Haugen, J.S. Sanders, I. Stolte-Dijkstra, D.A. Mans, E.J. Steenbergen, B.C. Hamel, M. Matignon, R. PfundtC. Jeanpierre, H. Boman, E. Rǿdahl, J.A. Veltman, P.M. Knappskog, V.V.A.M. Knoers, R. Roepman, H.H. Arts

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

Translated title of the contribution	Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19
Original language	Undefined/Unknown
Pages (from-to)	634-643
Number of pages	10
Journal	American Journal of Human Genetics
Volume	89
Issue number	5
Publication status	Published - 2011

Cite this

Bredrup, C., Saunier, S., Oud, M. M., Fiskerstrand, T., Hoischen, A., Brackman, D., Leh, S. M., Midtbǿ, M., Filhol, E., Bole-Feysot, C., Nitschké, P., Gilissen, C., Haugen, O. H., Sanders, J. S., Stolte-Dijkstra, I., Mans, D. A., Steenbergen, E. J., Hamel, B. C., Matignon, M., ... Arts, H. H. (2011). Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19. American Journal of Human Genetics, 89(5), 634-643.

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title = "Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19",

author = "C. Bredrup and S. Saunier and M.M. Oud and T. Fiskerstrand and A. Hoischen and D. Brackman and S.M. Leh and M. Midtbǿ and E. Filhol and C. Bole-Feysot and P. Nitschk{\'e} and C. Gilissen and O.H. Haugen and J.S. Sanders and I. Stolte-Dijkstra and D.A. Mans and E.J. Steenbergen and B.C. Hamel and M. Matignon and R. Pfundt and C. Jeanpierre and H. Boman and E. Rǿdahl and J.A. Veltman and P.M. Knappskog and V.V.A.M. Knoers and R. Roepman and H.H. Arts",

year = "2011",

language = "Undefined/Unknown",

volume = "89",

pages = "634--643",

journal = "American Journal of Human Genetics",

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Bredrup, C, Saunier, S, Oud, MM, Fiskerstrand, T, Hoischen, A, Brackman, D, Leh, SM, Midtbǿ, M, Filhol, E, Bole-Feysot, C, Nitschké, P, Gilissen, C, Haugen, OH, Sanders, JS, Stolte-Dijkstra, I, Mans, DA, Steenbergen, EJ, Hamel, BC, Matignon, M, Pfundt, R, Jeanpierre, C, Boman, H, Rǿdahl, E, Veltman, JA, Knappskog, PM, Knoers, VVAM, Roepman, R & Arts, HH 2011, 'Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19', American Journal of Human Genetics, vol. 89, no. 5, pp. 634-643.

TY - JOUR

T1 - Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19

AU - Bredrup, C.

AU - Saunier, S.

AU - Oud, M.M.

AU - Fiskerstrand, T.

AU - Hoischen, A.

AU - Brackman, D.

AU - Leh, S.M.

AU - Midtbǿ, M.

AU - Filhol, E.

AU - Bole-Feysot, C.

AU - Nitschké, P.

AU - Gilissen, C.

AU - Haugen, O.H.

AU - Sanders, J.S.

AU - Stolte-Dijkstra, I.

AU - Mans, D.A.

AU - Steenbergen, E.J.

AU - Hamel, B.C.

AU - Matignon, M.

AU - Pfundt, R.

AU - Jeanpierre, C.

AU - Boman, H.

AU - Rǿdahl, E.

AU - Veltman, J.A.

AU - Knappskog, P.M.

AU - Knoers, V.V.A.M.

AU - Roepman, R.

AU - Arts, H.H.

PY - 2011

Y1 - 2011

M3 - Article

SN - 0002-9297

VL - 89

SP - 634

EP - 643

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 5

ER -