Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly

B. W.M. Van Bon; A. Hoischen; J. Hehir-Kwa; A. P.M. De Brouwer; C. Ruivenkamp; A. C.J. Gijsbers; C. L. Marcelis; N. De Leeuw; J. A. Veltman; H. G. Brunner; B. B.A. De Vries

doi:10.1111/j.1399-0004.2010.01544.x

Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly

B. W.M. Van Bon
, A. Hoischen
, J. Hehir-Kwa
, A. P.M. De Brouwer
, C. Ruivenkamp
, A. C.J. Gijsbers
, C. L. Marcelis
, N. De Leeuw
, J. A. Veltman
, H. G. Brunner
, B. B.A. De Vries

Research output: Contribution to journal › Letter › peer-review

96 Citations (Scopus)

Original language	English
Pages (from-to)	296-299
Number of pages	4
Journal	Clinical Genetics
Volume	79
Issue number	3
DOIs	https://doi.org/10.1111/j.1399-0004.2010.01544.x
Publication status	Published - Mar 2011
Externally published	Yes

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10.1111/j.1399-0004.2010.01544.x

Cite this

@article{364b7a38d17c4aa4b8729d9c91200c45,

title = "Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly",

author = "\{Van Bon\}, \{B. W.M.\} and A. Hoischen and J. Hehir-Kwa and \{De Brouwer\}, \{A. P.M.\} and C. Ruivenkamp and Gijsbers, \{A. C.J.\} and Marcelis, \{C. L.\} and \{De Leeuw\}, N. and Veltman, \{J. A.\} and Brunner, \{H. G.\} and \{De Vries\}, \{B. B.A.\}",

year = "2011",

month = mar,

doi = "10.1111/j.1399-0004.2010.01544.x",

language = "English",

volume = "79",

pages = "296--299",

journal = "Clinical Genetics",

issn = "0009-9163",

publisher = "Wiley-Blackwell Publishing Ltd",

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T1 - Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly

AU - Van Bon, B. W.M.

AU - Hoischen, A.

AU - Hehir-Kwa, J.

AU - De Brouwer, A. P.M.

AU - Ruivenkamp, C.

AU - Gijsbers, A. C.J.

AU - Marcelis, C. L.

AU - De Leeuw, N.

AU - Veltman, J. A.

AU - Brunner, H. G.

AU - De Vries, B. B.A.

PY - 2011/3

Y1 - 2011/3

UR - https://www.scopus.com/pages/publications/79551646485

U2 - 10.1111/j.1399-0004.2010.01544.x

DO - 10.1111/j.1399-0004.2010.01544.x

M3 - Letter

C2 - 21294719

AN - SCOPUS:79551646485

SN - 0009-9163

VL - 79

SP - 296

EP - 299

JO - Clinical Genetics

JF - Clinical Genetics

IS - 3

ER -