Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects

C.M.R. Weemaes, M.J.D. van Tol, J. Wang, M. Dam, M.C.J.A. van Eggermond, P.E. Thijssen, C. Aytekin, N. Brunetti-Pierri, M. van der Burg, E. Graham Davies, A. Ferster, D. Furthner, G. Gimelli, A. Gennery, B. Kloeckener-Gruissem, S. Meyn, C. Powell, I. Reisli, C. Schuetz, A. Schulz & 3 others A. Shugar, P.J. van den Elsen, S.M. van der Maarel

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)1219-1225
JournalEuropean Journal of Human Genetics
Volume21
Issue number11
DOIs
Publication statusPublished - 2013

Cite this

Weemaes, C. M. R., van Tol, M. J. D., Wang, J., Dam, M., van Eggermond, M. C. J. A., Thijssen, P. E., ... van der Maarel, S. M. (2013). Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects. European Journal of Human Genetics, 21(11), 1219-1225. https://doi.org/10.1038/ejhg.2013.40
Weemaes, C.M.R. ; van Tol, M.J.D. ; Wang, J. ; Dam, M. ; van Eggermond, M.C.J.A. ; Thijssen, P.E. ; Aytekin, C. ; Brunetti-Pierri, N. ; van der Burg, M. ; Graham Davies, E. ; Ferster, A. ; Furthner, D. ; Gimelli, G. ; Gennery, A. ; Kloeckener-Gruissem, B. ; Meyn, S. ; Powell, C. ; Reisli, I. ; Schuetz, C. ; Schulz, A. ; Shugar, A. ; van den Elsen, P.J. ; van der Maarel, S.M. / Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects. In: European Journal of Human Genetics. 2013 ; Vol. 21, No. 11. pp. 1219-1225.
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title = "Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects",
author = "C.M.R. Weemaes and {van Tol}, M.J.D. and J. Wang and M. Dam and {van Eggermond}, M.C.J.A. and P.E. Thijssen and C. Aytekin and N. Brunetti-Pierri and {van der Burg}, M. and {Graham Davies}, E. and A. Ferster and D. Furthner and G. Gimelli and A. Gennery and B. Kloeckener-Gruissem and S. Meyn and C. Powell and I. Reisli and C. Schuetz and A. Schulz and A. Shugar and {van den Elsen}, P.J. and {van der Maarel}, S.M.",
year = "2013",
doi = "10.1038/ejhg.2013.40",
language = "Undefined/Unknown",
volume = "21",
pages = "1219--1225",
journal = "European Journal of Human Genetics",
issn = "1018-4813",
publisher = "Nature Publishing Group",
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Weemaes, CMR, van Tol, MJD, Wang, J, Dam, M, van Eggermond, MCJA, Thijssen, PE, Aytekin, C, Brunetti-Pierri, N, van der Burg, M, Graham Davies, E, Ferster, A, Furthner, D, Gimelli, G, Gennery, A, Kloeckener-Gruissem, B, Meyn, S, Powell, C, Reisli, I, Schuetz, C, Schulz, A, Shugar, A, van den Elsen, PJ & van der Maarel, SM 2013, 'Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects' European Journal of Human Genetics, vol. 21, no. 11, pp. 1219-1225. https://doi.org/10.1038/ejhg.2013.40

Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects. / Weemaes, C.M.R.; van Tol, M.J.D.; Wang, J.; Dam, M.; van Eggermond, M.C.J.A.; Thijssen, P.E.; Aytekin, C.; Brunetti-Pierri, N.; van der Burg, M.; Graham Davies, E.; Ferster, A.; Furthner, D.; Gimelli, G.; Gennery, A.; Kloeckener-Gruissem, B.; Meyn, S.; Powell, C.; Reisli, I.; Schuetz, C.; Schulz, A.; Shugar, A.; van den Elsen, P.J.; van der Maarel, S.M.

In: European Journal of Human Genetics, Vol. 21, No. 11, 2013, p. 1219-1225.

Research output: Contribution to journalArticleAcademicpeer-review

TY - JOUR

T1 - Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects

AU - Weemaes, C.M.R.

AU - van Tol, M.J.D.

AU - Wang, J.

AU - Dam, M.

AU - van Eggermond, M.C.J.A.

AU - Thijssen, P.E.

AU - Aytekin, C.

AU - Brunetti-Pierri, N.

AU - van der Burg, M.

AU - Graham Davies, E.

AU - Ferster, A.

AU - Furthner, D.

AU - Gimelli, G.

AU - Gennery, A.

AU - Kloeckener-Gruissem, B.

AU - Meyn, S.

AU - Powell, C.

AU - Reisli, I.

AU - Schuetz, C.

AU - Schulz, A.

AU - Shugar, A.

AU - van den Elsen, P.J.

AU - van der Maarel, S.M.

PY - 2013

Y1 - 2013

U2 - 10.1038/ejhg.2013.40

DO - 10.1038/ejhg.2013.40

M3 - Article

VL - 21

SP - 1219

EP - 1225

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

SN - 1018-4813

IS - 11

ER -