A carregar...
Kagami-Ogata Syndrome: Case Series and Review of Literature
Kagami-Ogata syndrome (KOS) (OMIM #608149) is a genetic imprinting disorder affecting chromosome 14 that results in a characteristic phenotype consisting of typical facial features, skeletal abnormalities including rib abnormalities described as “coat hanger ribs,” respiratory distress, abdominal wa...
Na minha lista:
| Publicado no: | AJP Rep |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Thieme Medical Publishers, Inc.
2021
|
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8159623/ https://ncbi.nlm.nih.gov/pubmed/34055463 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0041-1727287 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|