%0 Journal Article
%T Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum Disorder
%A Alain Verloes
%A Audrey Labalme
%A Brigitte Gilbert-Dussardier
%A Caroline Demily
%A Caroline Schluth-Bolard
%A Damien Sanlaville
%A Fabienne Giuliano
%A Gaetan Lesca
%A Giuseppe Testa
%A Julie Masson
%A Massimiliano Rossi
%A Nicolas Chatron
%A Patrick Edery
%A Pierre-Antoine Rollat-Farnier
%A Renaud Touraine
%A Sylvie Tordjman
%J Archive of "Orphanet Journal of Rare Diseases".
%D 2019
%R 10.1186/s13023-019-1094-5
%X The online version of this article (10.1186/s13023-019-1094-5) contains supplementary material, which is available to authorized users
%K Autism Spectrum Disorder
%K Williams Beuren syndrome
%K 7q11.23 microdeletion
%K GTF2I
%K Whole exome sequencing
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6545013/