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Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex
The phenotype currently accepted as Pierre Robin syndrome/sequence/anomalad/complex (PR) is characterized by mandibular dysmorphology, glossoptosis, respiratory obstruction, and in some cases, cleft palate. A causative sequence of developmental events is hypothesized for PR, but few clear causal rel...
Guardat en:
| Publicat a: | J Dev Biol |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
MDPI
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7768358/ https://ncbi.nlm.nih.gov/pubmed/33291480 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jdb8040030 |
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