Article
Clinical findings and phenotype in a toddler with 48,XXYY syndrome.
American journal of medical genetics. Part A - 15 Jun 2003
Demirhan Osman
Abstract excerpt
No abstract is available from the source.
Topics
- Chromosomes, Human, X
- Chromosomes, Human, Y
- Developmental Disabilities
- Follow-Up Studies
- Humans
- Infant
- Intellectual Disability
- Male
- Phenotype
- Sex Chromosome Aberrations
- Syndrome
