Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorder
Carter, MT, Nikkel, SM, Fernandez, BA, Marshall, CR, Noor, A, Lionel, AC, Prasad, A, Pinto, D, Joseph-George, AM, Noakes, C, Fairbrother-Davies, C, Roberts, W, Vincent, J, Weksberg, R, Scherer, SW
Published in Clinical genetics (01.11.2011)
Published in Clinical genetics (01.11.2011)
Get full text
Journal Article
Congenital Arthrogryposis : An Extension of the 15q11.2 BP1-BP2 Microdeletion Syndrome?
Williams, C. A., Fairbrother, L. C., Usrey, K. M., Butler, Merlin G., Dasouki, Majed
Published in Case reports in genetics (01.01.2014)
Published in Case reports in genetics (01.01.2014)
Get full text
Journal Article