Novel BCOR mutations in patients with oculofaciocardiodental (OFCD) syndrome

H. E. Feberwee; I. Feenstra; S. Oberoi; I. E. Sama; C. W. Ockeloen; F. Clum; A. Slavotinek; M. A R Kuijpers; D. Dooijes; A. M. Kuijpers-Jagtman; T. Kleefstra; C. E L Carels

doi:10.1111/cge.12125

Novel BCOR mutations in patients with oculofaciocardiodental (OFCD) syndrome

H. E. Feberwee, I. Feenstra, S. Oberoi, I. E. Sama, C. W. Ockeloen, F. Clum, A. Slavotinek, M. A R Kuijpers, D. Dooijes, A. M. Kuijpers-Jagtman, T. Kleefstra, C. E L Carels^*

^*Corresponding author for this work

Section genome diagnostics

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

1 Citation (Scopus)

Original language	English
Pages (from-to)	194-197
Number of pages	4
Journal	Clinical Genetics
Volume	85
Issue number	2
DOIs	https://doi.org/10.1111/cge.12125
Publication status	Published - 1 Feb 2014

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10.1111/cge.12125

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@article{8782d4fba3ef4d8e9ae53057af03aaa9,

title = "Novel BCOR mutations in patients with oculofaciocardiodental (OFCD) syndrome",

author = "Feberwee, \{H. E.\} and I. Feenstra and S. Oberoi and Sama, \{I. E.\} and Ockeloen, \{C. W.\} and F. Clum and A. Slavotinek and Kuijpers, \{M. A R\} and D. Dooijes and Kuijpers-Jagtman, \{A. M.\} and T. Kleefstra and Carels, \{C. E L\}",

year = "2014",

month = feb,

day = "1",

doi = "10.1111/cge.12125",

language = "English",

volume = "85",

pages = "194--197",

journal = "Clinical Genetics",

issn = "0009-9163",

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T1 - Novel BCOR mutations in patients with oculofaciocardiodental (OFCD) syndrome

AU - Feberwee, H. E.

AU - Feenstra, I.

AU - Oberoi, S.

AU - Sama, I. E.

AU - Ockeloen, C. W.

AU - Clum, F.

AU - Slavotinek, A.

AU - Kuijpers, M. A R

AU - Dooijes, D.

AU - Kuijpers-Jagtman, A. M.

AU - Kleefstra, T.

AU - Carels, C. E L

PY - 2014/2/1

Y1 - 2014/2/1

UR - https://www.scopus.com/pages/publications/84892480279

U2 - 10.1111/cge.12125

DO - 10.1111/cge.12125

M3 - Article

C2 - 23557072

AN - SCOPUS:84892480279

SN - 0009-9163

VL - 85

SP - 194

EP - 197

JO - Clinical Genetics

JF - Clinical Genetics

IS - 2

ER -

Novel BCOR mutations in patients with oculofaciocardiodental (OFCD) syndrome

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