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Author/Creator Brockmann, K

1. Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?. (19th April 2013)

Authors:
Shoukier, M; Klein, N; Auber, B; Wickert, J; Schröder, J; Zoll, B; Burfeind, P; Bartels, I; Alsat, EA; Lingen, M; Grzmil, P; Schulze, S; Keyser, J; Weise, D; Borchers, M; Hobbiebrunken, E; Röbl, M; Gärtner, J; Brockmann, K; Zirn, B
Journal:
Clinical genetics
Issue:
Volume 83:Number 1(2013:Jan.)
Page Start:
53
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?. (21st February 2012)

Authors:
Shoukier, M; Klein, N; Auber, B; Wickert, J; Schröder, J; Zoll, B; Burfeind, P; Bartels, I; Alsat, EA; Lingen, M; Grzmil, P; Schulze, S; Keyser, J; Weise, D; Borchers, M; Hobbiebrunken, E; Röbl, M; Gärtner, J; Brockmann, K; Zirn, B
Journal:
Clinical genetics
Issue:
Volume 83:Number 1(2013:Jan.)
Page Start:
53
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗