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You searched for: Author/Creator Oliveira, Guiomar

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1. Analysis of Highly Conserved Regions of the 3'UTR of MECP2 Gene in Patients with Clinical Diagnosis of Rett Syndrome and Other Disorders Associated with Mental Retardation. Issue 6 (2008)

2. Definition of a putative pathological region in PARK2 associated with autism spectrum disorder through in silico analysis of its functional structure. (April 2017)

4. Identification of novel genetic causes of Rett syndrome-like phenotypes by whole exome sequencing. Issue 47 (December 2015)

5. Identification of novel genetic causes of Rett syndrome-like phenotypes. Issue 3 (6th January 2016)

6. ISDN2014_0322: REMOVED: Identification of novel genetic causes of Rett syndrome‐like phenotypes by whole exome sequencing. Issue 47 (5th November 2015)