The phenotype associated with a large deletion on MECP2. [electronic resource]
Producer: 20121226Description: 921-7 p. digitalISSN:- 1476-5438
- Adolescent
- Adult
- Age of Onset
- Australia -- epidemiology
- Base Sequence
- Child
- Child, Preschool
- Female
- Genetic Association Studies
- Genotype
- Humans
- Infant
- Male
- Methyl-CpG-Binding Protein 2 -- genetics
- Middle Aged
- Molecular Sequence Data
- Multiplex Polymerase Chain Reaction
- Phenotype
- Rett Syndrome -- diagnosis
- Sequence Deletion
- Severity of Illness Index
- Surveys and Questionnaires
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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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