Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype. [electronic resource]
Producer: 20130909Description: 822-8 p. digitalISSN:- 1552-4833
- Abnormalities, Multiple -- genetics
- Adult
- Child, Preschool
- Chromosome Deletion
- Chromosomes, Human, Pair 8
- Facies
- Female
- GATA4 Transcription Factor -- genetics
- Genome-Wide Association Study
- Heart Defects, Congenital -- diagnosis
- Humans
- Male
- Microsatellite Repeats
- Phenotype
- Polymorphism, Single Nucleotide
- User-Computer Interface
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Publication Type: Case Reports; Journal Article
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