A carregar...
Psychotic Features as the First Manifestation of 22q11.2 Deletion Syndrome
The 22q11.2 deletion is a genetic disorder which is characterized by abnormalities in cardiac functioning, facial structure, neurobehavioral development, T cell functioning, and velopharyngeal insufficiencies. In the presented case study, 22q11.2 deletion was found in a patient who has psychotic sym...
Na minha lista:
| Main Authors: | , , , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Korean Neuropsychiatric Association
2010
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2848773/ https://ncbi.nlm.nih.gov/pubmed/20396437 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4306/pi.2010.7.1.72 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|