Related Experiment Videos
Occurrence of 19p- in an infant with multiple dysmorphic features.
Annales De Genetique
|January 1, 1984
Summary
This case report details a partial deletion on chromosome 19 short arm. The patient presented with multiple dysmorphic features, highlighting a rare genetic condition.
Area of Science:
- Genetics
- Clinical Medicine
- Human Biology
Background:
- Chromosome 19 deletions are rare genetic abnormalities.
- Dysmorphic features can indicate underlying genetic disorders.