Further evidence that a 100 Kb critical region is responsible for developmental delay, seizures, and dysmorphic features in 1q43q44 deletion patients
Journal Articles
- Overview
- Research
- Identity
- Additional Document Info
- View All
Overview
status
publication date
- April 2013
has subject area
- 0604 Genetics (FoR)
- 1103 Clinical Sciences (FoR)
- Child (MeSH)
- Child, Preschool (MeSH)
- Chromosome Deletion (MeSH)
- Chromosomes, Human, Pair 1 (MeSH)
- Developmental Disabilities (MeSH)
- Face (MeSH)
- Female (MeSH)
- Genetic Association Studies (MeSH)
- Humans (MeSH)
- Male (MeSH)
- Phenotype (MeSH)
- Seizures (MeSH)