Differences in speech and language abilities between children with 22q11.2 deletion syndrome and children with phenotypic features of 22q11.2 deletion syndrome but without microdeletion. [electronic resource]
Producer: 20170329Description: 322-9 p. digitalISSN:- 1873-3379
- Cardiac Surgical Procedures
- Case-Control Studies
- Child
- Child, Preschool
- Chromosome Deletion
- Chromosomes, Human, Pair 22 -- genetics
- DiGeorge Syndrome -- epidemiology
- Female
- Genotype
- Heart Defects, Congenital -- epidemiology
- Humans
- In Situ Hybridization, Fluorescence
- Karyotype
- Language Development Disorders -- epidemiology
- Male
- Multiplex Polymerase Chain Reaction
- Phenotype
- Risk Factors
- Severity of Illness Index
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Publication Type: Journal Article
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