Microduplication 22q11.2 in a child with autism spectrum disorder: clinical and genetic study. [electronic resource]
Producer: 20090202Description: 953-5 p. digitalISSN:- 1469-8749
- Autistic Disorder -- diagnosis
- Cell Cycle Proteins -- genetics
- Child, Preschool
- Chromosomes, Human, Pair 22 -- genetics
- Consanguinity
- Developmental Disabilities -- diagnosis
- DiGeorge Syndrome -- diagnosis
- Diagnosis, Differential
- Gene Duplication
- Genetic Heterogeneity
- Histone Chaperones
- Humans
- In Situ Hybridization, Fluorescence
- Male
- Phenotype
- Transcription Factors -- genetics
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Publication Type: Case Reports; Journal Article
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