Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders. [electronic resource]
Producer: 20130104Description: 1619-22 p. digitalISSN:- 1095-9203
- Cephalometry
- Child
- Child Development Disorders, Pervasive -- genetics
- Child, Preschool
- Chromatin Assembly and Disassembly
- Cohort Studies
- DNA Probes
- DNA-Binding Proteins -- genetics
- Exome
- Female
- Genetic Association Studies
- Genetic Predisposition to Disease
- Humans
- Male
- Megalencephaly -- genetics
- Microcephaly -- genetics
- Mutation
- Nuclear Proteins -- genetics
- PTEN Phosphohydrolase -- genetics
- Protein Serine-Threonine Kinases -- genetics
- Protein-Tyrosine Kinases -- genetics
- Receptors, Cytoplasmic and Nuclear -- genetics
- Receptors, N-Methyl-D-Aspartate -- genetics
- Repressor Proteins -- genetics
- Sequence Analysis, DNA -- methods
- T-Box Domain Proteins -- genetics
- Transcription Factors -- genetics
- beta Catenin -- genetics
- Dyrk Kinases
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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