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- Correlações Entre O Fenótipo Na Síndrome De Williams E Os Genes Deletados
- From Williams Syndrome to Musical Genes
- A Human-Specific Structural Variation at the ZNF558 Locus Controls A
- Induction of Therapeutic Tissue Tolerance Foxp3 Expression Is
- Copy Number Variants at Williams–Beuren Syndrome 7Q11.23 Region
- Williams–Beuren Syndrome
- Williams-Beuren Syndrome Locus: a Model of CNV Affecting Gene Dosage and Phenotypes Professor Lucy R
- Oxidative Stress in Down and Williams-Beuren Syndromes: an Overview
- Alcohol 48 (2014) 603E610
- Defining the Effect of the 16P11.2 Duplication on Cognition, Behavior, and Medical Comorbidities
- European Sea Bass Genome and Its Variation Provide Insights Into Adaptation to Euryhalinity and Speciation
- Neuronal Deletion of Gtf2i, Associated with Williams Syndrome, Causes Behavioral and Myelin Alterations Rescuable by a Remyelinating Drug
- Global Analysis of Gene Expression in the Developing Brain of Gtf2ird1
- Beuren Syndrome
- MCAT Mutations Cause Nuclear LHON-Like Optic Neuropathy
- Systematic Review Manuscript.Pdf