Published in
BioMed Central, Orphanet Journal of Rare Diseases, 1(14), 2019
DOI: 10.1186/s13023-019-1094-5
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Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum Disorder
Journal article published in 2019 by
Julie Masson,
Caroline Demily,
Nicolas Chatron,
Audrey Labalme,
Pierre-Antoine Rollat-Farnier,
Caroline Schluth-Bolard,
Brigitte Gilbert-Dussardier,
Fabienne Giuliano,
Renaud Touraine,
Sylvie Tordjman,
Alain Verloes,
Giuseppe Testa,
Damien Sanlaville,
Patrick Edery,
Gaetan Lesca 
and other authors.
and other authors.
This paper is made freely available by the publisher.
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