Autism phenotype in genetic disorders, description of clinical characteristics and implications for the search for autism genes in the general population (2) 22q11.2 deletion syndrome

J.A.S. Vorstman; M.E.J. Sijmens-Morcus; W.G. Staal; E. van Daalen; M.V. de Jonge; P. Meyer; B.S. Emanuel; R.S. Kahn; F.A. Beemer; H. van Engeland

Autism phenotype in genetic disorders, description of clinical characteristics and implications for the search for autism genes in the general population (2) 22q11.2 deletion syndrome

Translated title of the contribution: Autism phenotype in genetic disorders, description of clinical characteristics and implications for the search for autism genes in the general population (2) 22q11.2 deletion syndrome

J.A.S. Vorstman, M.E.J. Sijmens-Morcus, W.G. Staal, E. van Daalen, M.V. de Jonge, P. Meyer, B.S. Emanuel, R.S. Kahn, F.A. Beemer, H. van Engeland

Research output: Contribution to conference › Poster › Other research output

Translated title of the contribution	Autism phenotype in genetic disorders, description of clinical characteristics and implications for the search for autism genes in the general population (2) 22q11.2 deletion syndrome
Original language	Undefined/Unknown
Publication status	Published - 7 Oct 2007
Event	XVth World Congress on Psychiatric Genetics: Bridging genes to behaviour - New York Duration: 7 Oct 2007 → 11 Oct 2007

Conference

Conference	XVth World Congress on Psychiatric Genetics: Bridging genes to behaviour
City	New York
Period	7/10/07 → 11/10/07

Cite this

Vorstman, J. A. S., Sijmens-Morcus, M. E. J., Staal, W. G., van Daalen, E., de Jonge, M. V., Meyer, P., Emanuel, B. S., Kahn, R. S., Beemer, F. A., & van Engeland, H. (2007). Autism phenotype in genetic disorders, description of clinical characteristics and implications for the search for autism genes in the general population (2) 22q11.2 deletion syndrome. Poster session presented at XVth World Congress on Psychiatric Genetics: Bridging genes to behaviour, New York.

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title = "Autism phenotype in genetic disorders, description of clinical characteristics and implications for the search for autism genes in the general population (2) 22q11.2 deletion syndrome",

author = "J.A.S. Vorstman and M.E.J. Sijmens-Morcus and W.G. Staal and \{van Daalen\}, E. and \{de Jonge\}, M.V. and P. Meyer and B.S. Emanuel and R.S. Kahn and F.A. Beemer and \{van Engeland\}, H.",

note = "XVth World Congress on Psychiatric Genetics: Bridging genes to behaviour; XVth World Congress on Psychiatric Genetics: Bridging genes to behaviour ; Conference date: 07-10-2007 Through 11-10-2007",

year = "2007",

month = oct,

day = "7",

language = "Undefined/Unknown",

}

Vorstman, JAS, Sijmens-Morcus, MEJ, Staal, WG, van Daalen, E, de Jonge, MV, Meyer, P, Emanuel, BS, Kahn, RS, Beemer, FA & van Engeland, H 2007, 'Autism phenotype in genetic disorders, description of clinical characteristics and implications for the search for autism genes in the general population (2) 22q11.2 deletion syndrome', XVth World Congress on Psychiatric Genetics: Bridging genes to behaviour, New York, 7/10/07 - 11/10/07.

Autism phenotype in genetic disorders, description of clinical characteristics and implications for the search for autism genes in the general population (2) 22q11.2 deletion syndrome. / Vorstman, J.A.S.; Sijmens-Morcus, M.E.J.; Staal, W.G. et al.
2007. Poster session presented at XVth World Congress on Psychiatric Genetics: Bridging genes to behaviour, New York.

Research output: Contribution to conference › Poster › Other research output

TY - CONF

T1 - Autism phenotype in genetic disorders, description of clinical characteristics and implications for the search for autism genes in the general population (2) 22q11.2 deletion syndrome

AU - Vorstman, J.A.S.

AU - Sijmens-Morcus, M.E.J.

AU - Staal, W.G.

AU - van Daalen, E.

AU - de Jonge, M.V.

AU - Meyer, P.

AU - Emanuel, B.S.

AU - Kahn, R.S.

AU - Beemer, F.A.

AU - van Engeland, H.

N1 - XVth World Congress on Psychiatric Genetics: Bridging genes to behaviour

PY - 2007/10/7

Y1 - 2007/10/7

M3 - Poster

T2 - XVth World Congress on Psychiatric Genetics: Bridging genes to behaviour

Y2 - 7 October 2007 through 11 October 2007

ER -

Vorstman JAS, Sijmens-Morcus MEJ, Staal WG, van Daalen E, de Jonge MV, Meyer P et al.. Autism phenotype in genetic disorders, description of clinical characteristics and implications for the search for autism genes in the general population (2) 22q11.2 deletion syndrome. 2007. Poster session presented at XVth World Congress on Psychiatric Genetics: Bridging genes to behaviour, New York.