Biblio

Found 2 results

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2010

[1802] Bilguvar, K., Ozturk A K., Louvi A., Kwan K. Y., Choi M., Tatli B., et al. (2010). Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations. Nature. advance online publication,

2008

[857] Stillman, A. A., Bakkaloglu B., O'Roak B. J., Louvi A., Gupta A. R., Abelson J. F., et al. (2008). Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorders. The American Journal of Human Genetics. 82(1), 165 - 173.