3q29 interstitial microdeletion syndrome: an inherited case associated with cardiac defect and normal cognition.

Li, Feng

3q29 interstitial microdeletion syndrome: an inherited case associated with cardiac defect and normal cognition. [electronic resource] - European journal of medical genetics - 349-52 p. digital

Publication Type: Case Reports; Journal Article

1878-0849

10.1016/j.ejmg.2009.05.001 doi


Adult
Aortic Stenosis, Subvalvular--genetics
Cells, Cultured
Chromosome Breakage
Chromosome Deletion
Chromosomes, Artificial, Bacterial
Chromosomes, Human, Pair 3
Cognition
Comparative Genomic Hybridization
Databases as Topic
Ductus Arteriosus, Patent--genetics
Fathers
Humans
In Situ Hybridization, Fluorescence
Infant
Lymphocytes--cytology
Male
Syndrome