Towards earlier diagnosis of 22q11 deletions. [electronic resource]
Producer: 20000119Description: 513-4 p. digitalISSN:- 1468-2044
- Abnormalities, Multiple -- diagnosis
- Adolescent
- Adult
- Child
- Child, Preschool
- Chromosome Deletion
- Chromosomes, Human, Pair 22
- Craniofacial Abnormalities -- diagnosis
- DiGeorge Syndrome -- genetics
- Heart Defects, Congenital -- diagnosis
- Humans
- In Situ Hybridization, Fluorescence
- Infant
- Infant, Newborn
- Male
- Tetralogy of Fallot -- genetics
- Time Factors
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Publication Type: Journal Article
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