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.

Authors :: Leeuw, N. de
Pfundt, R.P.
Koolen, D.A.
Neefs, I.
Scheltinga, I.
Mieloo, H.
Sistermans, E.A.
Nillesen, W.M.
Smeets, D.F.C.M.
Vries, L.B.A. de
Knoers, N.V.A.M.
Leeuw, N. de
Pfundt, R.P.
Koolen, D.A.
Neefs, I.
Scheltinga, I.
Mieloo, H.
Sistermans, E.A.
Nillesen, W.M.
Smeets, D.F.C.M.
Vries, L.B.A. de
Knoers, N.V.A.M.
Source :: Journal of Medical Genetics; 122; 124; 0022-2593; 2; 45; ~Journal of Medical Genetics~122~124~~~0022-2593~2~45~~
Publication Year :: 2008
Abstract: Contains fulltext : 69185.pdf (publisher's version ) (Closed access)

Database :: OAIster
Journal :: Journal of Medical Genetics; 122; 124; 0022-2593; 2; 45; ~Journal of Medical Genetics~122~124~~~0022-2593~2~45~~
Publication Type :: Electronic Resource
Accession number :: edsoai.on1284157482
Document Type :: Electronic Resource

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