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Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.
Published in:
Molecular Autism, 2013, v. 4, n. 1, p. 1, doi. 10.1186/2040-2392-4-18
By:
- Soorya, Latha;
- Kolevzon, Alexander;
- Zweifach, Jessica;
- Lim, Teresa;
- Dobry, Yuriy;
- Schwartz, Lily;
- Frank, Yitzchak;
- Ting Wang, A.;
- Cai, Guiqing;
- Parkhomenko, Elena;
- Halpern, Danielle;
- Grodberg, David;
- Angarita, Benjamin;
- Willner, Judith P.;
- Yang, Amy;
- Canitano, Roberto;
- Chaplin, William;
- Betancur, Catalina;
- Buxbaum, Joseph D.
Publication type:
Article
De novo SCN2A splice site mutation in a boy with Autism spectrum disorder.
Published in:
BMC Medical Genetics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2350-15-35
By:
- Tavassoli, Teresa;
- Kolevzon, Alexander;
- Wang, A. Ting;
- Curchack-Lichtin, Jocelyn;
- Halpern, Danielle;
- Schwartz, Lily;
- Soffes, Sarah;
- Bush, Lauren;
- Grodberg, David;
- Guiqing Cai;
- Buxbaum, Joseph D.
Publication type:
Article