ITEM METADATA RECORD
Title: Complex inheritance of a rare microdeletion and low frequency regulatory SNP cause TAR syndrome. A model for other microdeletion disorders
Authors: Newbury-Ecob, Ruth
Albers, C. A
Paul, D. S
Schulze, H
Freson, Kathleen
Stephens, J. C
Smith, K
Williams, M
Ouwehand, W. H
Ghevaert, C
Issue Date: 2012
Publisher: BMJ Publishing Group
Host Document: Journal of Medical Genetics vol:49 pages:S38-S38
Conference: British Human Genetics Conference location:Coventry: ENGLAND date:SEP 17-19, 2012
ISSN: 0022-2593
Publication status: published
KU Leuven publication type: IMa
Appears in Collections:Molecular and Vascular Biology

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