News dal Mondo

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.

30 gen , 2014 News dal Mondo

Hum Mol Genet. 2014 Gen 14. Authors Lionel AC1, Tammimies K, Vaags AK, Rosenfeld JA, Ahn JW, Merico D, Noor A, Runke CK, Pillalamarri VK, Carter MT, Gazzellone MJ, Thiruvahindrapuram B,Fagerberg C, Laulund LW, Pellecchia G, Lamoureux S, Deshpande C, Clayton-Smith J, White […]

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Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testing

3 giu , 2013 News dal Mondo

European Journal of Human Genetics advance online publication 22 May 2013 Joanna Wiszniewska1, Weimin Bi1, Chad Shaw1, Pawel Stankiewicz1, Sung-Hae L Kang2, Amber N Pursley1, Seema Lalani1,3, Patricia Hixson1, Tomasz Gambin4, Chun-hui Tsai5,6, Hans-Georg Bock7, Maria Descartes8, Frank J Probst1,3, Fernando Scaglia1, […]

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Custom oligonucleotide array-based CGH: a reliable diagnostic tool for detection of exonic copy-number changes in multiple targeted genes

30 mag , 2013 News dal Mondo

Aurélie Vasson1, Céline Leroux1, Lucie Orhant1, Mathieu Boimard1, Aurélie Toussaint1, Chrystel Leroy1, Virginie Commere1, Tiffany Ghiotti1, Nathalie Deburgrave1, Yoann Saillour2, Isabelle Atlan1, Corinne Fouveaut1, Cherif Beldjord1,2, Sophie Valleix1,2, France Leturcq1,2, Catherine Dodé1,2, Thierry Bienvenu1,2, Jamel Chelly1,2 and Mireille Cossée1,2 1Assistance Publique-Hôpitaux de Paris, Laboratoire de […]

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