DSpace

DSpace at RU >    University Library >    Academic bibliography >

SFX Query

Title: A newly recognised microdeletion syndrome involving 2p15p16.1: narrowing down the critical region by adding another patient detected by genome wide tiling path array comparative genomic hybridisation analysis.
Author(s): Leeuw, N. de (181941376)
Pfundt, R.P. (197470386)
Koolen, D.A. (298208490)
Neefs, I.
Scheltinga, I.
Mieloo, H.
Sistermans, E.A. (14900107X)
Nillesen, W.
Smeets, D.F.C.M. (094500436)
Vries, L.B.A. de (157142396)
Knoers, N.V.A.M. (298974460)
Publication year: 2008
Document type: Article / Letter to editor
Journal: Journal of Medical Genetics
ISSN: 1468-6244
Volume: vol. 45
Issue: iss. 2
Start page: p. 122
End page: p. 124
Subject: UMCN 3.2: Cognitive neurosciences
UMCN 5.1: Genetic defects of metabolism
Organization: Human Genetics
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/69185

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

  DSpace Software Copyright © 2002-2011  Duraspace - Feedback