A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms
Hladilkova, Eva; Barøy, Tuva; Fannemel, Madeleine; Vallova, Vladimira; Misceo, Doriana; Bryn, Vesna; Slamova, Iva; Prasilova, Sarka; Kuglik, Petr; Frengen, Eirik
Journal article; PublishedVersion; Peer reviewed
View/ Open
Year
2015Permanent link
http://urn.nb.no/Metadata
Show metadataAppears in the following Collection
- Institutt for klinisk medisin [10814]
- BioMed Central høstingsarkiv [3217]