ALK2 mutation in a patient with Down's syndrome and a congenital heart defect

I.C. Joziasse; K.A. Smith; S. Chocron; M. van Dinther; V. Guryev; J.J. van der Smagt; E.P.J.G. Cuppen; P. ten Dijke; B.J. Mulder; C.L. Maslen; B. Reshev; P.A.F.M. Doevendans; J. Bakkers

ALK2 mutation in a patient with Down's syndrome and a congenital heart defect

Translated title of the contribution: ALK2 mutation in a patient with Down's syndrome and a congenital heart defect

I.C. Joziasse, K.A. Smith, S. Chocron, M. van Dinther, V. Guryev, J.J. van der Smagt, E.P.J.G. Cuppen, P. ten Dijke, B.J. Mulder, C.L. Maslen, B. Reshev, P.A.F.M. Doevendans, J. Bakkers

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

Translated title of the contribution	ALK2 mutation in a patient with Down's syndrome and a congenital heart defect
Original language	Undefined/Unknown
Pages (from-to)	389-393
Number of pages	5
Journal	European Journal of Human Genetics
Volume	19
Issue number	4
Publication status	Published - 2011

Access to Document

http://www.ncbi.nlm.nih.gov/pubmed/21248739

Cite this

Joziasse, I. C., Smith, K. A., Chocron, S., van Dinther, M., Guryev, V., van der Smagt, J. J., Cuppen, E. P. J. G., ten Dijke, P., Mulder, B. J., Maslen, C. L., Reshev, B., Doevendans, P. A. F. M., & Bakkers, J. (2011). ALK2 mutation in a patient with Down's syndrome and a congenital heart defect. European Journal of Human Genetics, 19(4), 389-393. http://www.ncbi.nlm.nih.gov/pubmed/21248739

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title = "ALK2 mutation in a patient with Down's syndrome and a congenital heart defect",

author = "I.C. Joziasse and K.A. Smith and S. Chocron and {van Dinther}, M. and V. Guryev and {van der Smagt}, J.J. and E.P.J.G. Cuppen and {ten Dijke}, P. and B.J. Mulder and C.L. Maslen and B. Reshev and P.A.F.M. Doevendans and J. Bakkers",

year = "2011",

language = "Undefined/Unknown",

volume = "19",

pages = "389--393",

journal = "European Journal of Human Genetics",

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Joziasse, IC, Smith, KA, Chocron, S, van Dinther, M, Guryev, V, van der Smagt, JJ , Cuppen, EPJG, ten Dijke, P, Mulder, BJ, Maslen, CL, Reshev, B, Doevendans, PAFM & Bakkers, J 2011, 'ALK2 mutation in a patient with Down's syndrome and a congenital heart defect', European Journal of Human Genetics, vol. 19, no. 4, pp. 389-393. <http://www.ncbi.nlm.nih.gov/pubmed/21248739>

TY - JOUR

T1 - ALK2 mutation in a patient with Down's syndrome and a congenital heart defect

AU - Joziasse, I.C.

AU - Smith, K.A.

AU - Chocron, S.

AU - van Dinther, M.

AU - Guryev, V.

AU - van der Smagt, J.J.

AU - Cuppen, E.P.J.G.

AU - ten Dijke, P.

AU - Mulder, B.J.

AU - Maslen, C.L.

AU - Reshev, B.

AU - Doevendans, P.A.F.M.

AU - Bakkers, J.

PY - 2011

Y1 - 2011

M3 - Article

SN - 1018-4813

VL - 19

SP - 389

EP - 393

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 4

ER -