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CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1.
PLoS One. 2013;8(3):e59061. doi: 10.1371/journal.pone.0059061. Epub 2013 Mar 22.
PLoS One. 2013.
PMID: 23533600
Free PMC article.
Association of DRD2 variants and Gilles de la Tourette syndrome in a family-based sample from a South American population isolate.
Herzberg I, Valencia-Duarte AV, Kay VA, White DJ, Müller H, Rivas IC, Mesa SC, Cuartas M, García J, Bedoya G, Cornejo W, Ruiz-Linares A, Kremeyer B.
Herzberg I, et al. Among authors: rivas ic.
Psychiatr Genet. 2010 Aug;20(4):179-83. doi: 10.1097/YPG.0b013e32833a215a.
Psychiatr Genet. 2010.
PMID: 20431429
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[Clinical characterisation and power simulations to detect genetic linkage in attention deficit hyperactivity disorder in Antioquian families].
Cornejo W, Cuartas M, Gómez-Uribe LF, Carrizosa J, Rivas I, Castillo H, Bedoya G, Ruiz A.
Cornejo W, et al.
Rev Neurol. 2004 Feb 16-29;38(4):319-22.
Rev Neurol. 2004.
PMID: 14997454
Free article.
Spanish.
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[Transient Brown-Séquard syndrome due to spontaneous spinal epidural hematoma].
Narberhaus B, Rivas I, Vilalta J, Abós J, Ugarte A.
Narberhaus B, et al.
Neurologia. 2002 Aug-Sep;17(7):384-7.
Neurologia. 2002.
PMID: 12236959
Review.
Spanish.
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