Transmitted duplication of 8p23.1-8p23.2 associated with speech delay, autism and learning difficultiesGLANCY, Mary; BARNICOAT, Angela; BARBER, John C. K et al.European journal of human genetics. 2009, Vol 17, Num 1, pp 37-43, issn 1018-4813, 7 p.Article

Oto-facio-cervical (OFC) syndrome is a contiguous gene deletion syndrome involving EYA1: molecular analysis confirms allelism with BOR syndrome and further narrows the Duane syndrome critical region to 1 cmRICKARD, Sarah; PARKER, Michael; HOFF, William Van'T et al.Human genetics. 2001, Vol 108, Num 5, pp 398-403, issn 0340-6717Article

Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13)DE VRIES, Bert B. A; LEES, Melissa; KNIGHT, Samantha J. L et al.American journal of medical genetics. 2001, Vol 99, Num 4, pp 314-319, issn 0148-7299Article

Disruption of the bipartite imprinting center in a family with Angelman syndromeBUITING, Karin; BARNICOAT, Angela; LICH, Christina et al.American journal of human genetics. 2001, Vol 68, Num 5, pp 1290-1294, issn 0002-9297Article

Autism, language and communication in children with sex chromosome trisomiesBISHOP, Dorothy V. M; JACOBS, Patricia A; SHEARS, Deborah et al.Archives of disease in childhood. 2011, Vol 96, Num 10, pp 954-959, issn 0003-9888, 6 p.Article