Legius syndrome in fourteen families

E. Denayer; M. Chmara; H Brems; A.M. Kievit; Y. van Bever; A.M.W. van den Ouweland; R. van Minkelen; A. de Goede-Bolder; R. Oostenbrink; P. Lakeman; E. Beert; T. Ishizaki; T. Mori; K. Keymolen; J. van der Ende; E. Mangold; S. Peltonen; G. Brice; J. Rankin; K.Y. van Spaendonck-Zwarts; A. Yoshimura; E. Legius

doi:10.1002/humu.21404

Legius syndrome in fourteen families

E. Denayer, M. Chmara, H Brems, A.M. Kievit, Y. van Bever, A.M.W. van den Ouweland, R. van Minkelen, A. de Goede-Bolder, R. Oostenbrink, P. Lakeman, E. Beert, T. Ishizaki, T. Mori, K. Keymolen, J. van der Ende, E. Mangold, S. Peltonen, G. Brice, J. Rankin, K.Y. van Spaendonck-ZwartsA. Yoshimura, E. Legius

Clinical genetics

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

Original language	Undefined/Unknown
Pages (from-to)	E1985-E1998
Journal	Human Mutation
Volume	32
Issue number	1
DOIs	https://doi.org/10.1002/humu.21404
Publication status	Published - 2011

Access to Document

10.1002/humu.21404

Cite this

Denayer, E., Chmara, M., Brems, H., Kievit, A. M., van Bever, Y., van den Ouweland, A. M. W., van Minkelen, R., de Goede-Bolder, A., Oostenbrink, R., Lakeman, P., Beert, E., Ishizaki, T., Mori, T., Keymolen, K., van der Ende, J., Mangold, E., Peltonen, S., Brice, G., Rankin, J., ... Legius, E. (2011). Legius syndrome in fourteen families. Human Mutation, 32(1), E1985-E1998. https://doi.org/10.1002/humu.21404

Denayer, E. ; Chmara, M. ; Brems, H ; Kievit, A.M. ; van Bever, Y. ; van den Ouweland, A.M.W. ; van Minkelen, R. ; de Goede-Bolder, A. ; Oostenbrink, R. ; Lakeman, P. ; Beert, E. ; Ishizaki, T. ; Mori, T. ; Keymolen, K. ; van der Ende, J. ; Mangold, E. ; Peltonen, S. ; Brice, G. ; Rankin, J. ; van Spaendonck-Zwarts, K.Y. ; Yoshimura, A. ; Legius, E. / Legius syndrome in fourteen families. In: Human Mutation. 2011 ; Vol. 32, No. 1. pp. E1985-E1998.

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title = "Legius syndrome in fourteen families",

author = "E. Denayer and M. Chmara and H Brems and A.M. Kievit and {van Bever}, Y. and {van den Ouweland}, A.M.W. and {van Minkelen}, R. and {de Goede-Bolder}, A. and R. Oostenbrink and P. Lakeman and E. Beert and T. Ishizaki and T. Mori and K. Keymolen and {van der Ende}, J. and E. Mangold and S. Peltonen and G. Brice and J. Rankin and {van Spaendonck-Zwarts}, K.Y. and A. Yoshimura and E. Legius",

year = "2011",

doi = "10.1002/humu.21404",

language = "Undefined/Unknown",

volume = "32",

pages = "E1985--E1998",

journal = "Human Mutation",

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Denayer, E, Chmara, M, Brems, H, Kievit, AM, van Bever, Y, van den Ouweland, AMW, van Minkelen, R, de Goede-Bolder, A, Oostenbrink, R, Lakeman, P, Beert, E, Ishizaki, T, Mori, T, Keymolen, K, van der Ende, J, Mangold, E, Peltonen, S, Brice, G, Rankin, J, van Spaendonck-Zwarts, KY, Yoshimura, A & Legius, E 2011, 'Legius syndrome in fourteen families', Human Mutation, vol. 32, no. 1, pp. E1985-E1998. https://doi.org/10.1002/humu.21404

Legius syndrome in fourteen families. / Denayer, E.; Chmara, M.; Brems, H; Kievit, A.M.; van Bever, Y.; van den Ouweland, A.M.W.; van Minkelen, R.; de Goede-Bolder, A.; Oostenbrink, R.; Lakeman, P.; Beert, E.; Ishizaki, T.; Mori, T.; Keymolen, K.; van der Ende, J.; Mangold, E.; Peltonen, S.; Brice, G.; Rankin, J.; van Spaendonck-Zwarts, K.Y.; Yoshimura, A.; Legius, E.

In: Human Mutation, Vol. 32, No. 1, 2011, p. E1985-E1998.

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

TY - JOUR

T1 - Legius syndrome in fourteen families

AU - Denayer, E.

AU - Chmara, M.

AU - Brems, H

AU - Kievit, A.M.

AU - van Bever, Y.

AU - van den Ouweland, A.M.W.

AU - van Minkelen, R.

AU - de Goede-Bolder, A.

AU - Oostenbrink, R.

AU - Lakeman, P.

AU - Beert, E.

AU - Ishizaki, T.

AU - Mori, T.

AU - Keymolen, K.

AU - van der Ende, J.

AU - Mangold, E.

AU - Peltonen, S.

AU - Brice, G.

AU - Rankin, J.

AU - van Spaendonck-Zwarts, K.Y.

AU - Yoshimura, A.

AU - Legius, E.

PY - 2011

Y1 - 2011

U2 - 10.1002/humu.21404

DO - 10.1002/humu.21404

M3 - Article

C2 - 21089071

VL - 32

SP - E1985-E1998

JO - Human Mutation

JF - Human Mutation

SN - 1059-7794

IS - 1

ER -