Anatomic patterns of conotruncal defects associated with deletion 22q11. [electronic resource]
Producer: 20010927Description: 45-8 p. digitalISSN:- 1098-3600
- Abnormalities, Multiple -- genetics
- Adolescent
- Aorta, Thoracic -- abnormalities
- Child
- Child, Preschool
- Chromosome Deletion
- Chromosomes, Human, Pair 22
- DiGeorge Syndrome -- diagnosis
- Female
- Genotype
- Heart Defects, Congenital -- diagnosis
- Heart Septal Defects, Ventricular -- diagnosis
- Humans
- In Situ Hybridization, Fluorescence
- Infant
- Infant, Newborn
- Male
- Phenotype
- Pulmonary Atresia -- diagnosis
- Tetralogy of Fallot -- diagnosis
- Truncus Arteriosus -- abnormalities
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Publication Type: Journal Article
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