Article
A case of de novo mosaic 18q21.3 deletion with a mild phenotype.
Genetic counseling (Geneva, Switzerland) - 1 Jan 2014
Alp M Y, Cebi A H, Seyhan S, Cansu A, Ikbal M
Abstract excerpt
No abstract is available from the source.
Topics
- Child, Preschool
- Chromosome Deletion
- Chromosome Disorders
- Chromosomes, Human, Pair 18
- Developmental Disabilities
- Humans
- Male
- Mosaicism
- Phenotype
