A 17p11.2 germline deletion in a patient with Smith-Magenis syndrome and neuroblastoma

T. Hienonen; H. Sammalkorpi; P. Isohanni; R. Versteeg; R. Karikoski; L.A. Aaltonen

doi:https://doi.org/10.1136/jmg.2004.022814

A 17p11.2 germline deletion in a patient with Smith-Magenis syndrome and neuroblastoma

T. Hienonen, H. Sammalkorpi, P. Isohanni, R. Versteeg, R. Karikoski, L.A. Aaltonen

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

4 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	e3
Journal	Journal of medical genetics
Volume	42
Issue number	1
DOIs	https://doi.org/10.1136/jmg.2004.022814
Publication status	Published - 2005

Keywords

AMC wi-buiten

Access to Document

https://doi.org/10.1136/jmg.2004.022814

https://pure.uva.nl/ws/files/3896454/45833_207973y.pdf

Cite this

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title = "A 17p11.2 germline deletion in a patient with Smith-Magenis syndrome and neuroblastoma",

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AU - Hienonen, T.

AU - Sammalkorpi, H.

AU - Isohanni, P.

AU - Versteeg, R.

AU - Karikoski, R.

AU - Aaltonen, L.A.

N1 - Helsinki. Copyright: BMJ Publishing Group

PY - 2005

Y1 - 2005

KW - AMC wi-buiten

U2 - https://doi.org/10.1136/jmg.2004.022814

DO - https://doi.org/10.1136/jmg.2004.022814

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