Weill-Marchesani-like syndrome caused by an FBN1 mutation with low-penetrance

Detalles Bibliográficos
Autores principales: Yang, Guo-Yuan, Huang, Xi, Chen, Bing-Jie, Xu, Zhu-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Clinical Observations
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183799/
https://www.ncbi.nlm.nih.gov/pubmed/34075901
http://dx.doi.org/10.1097/CM9.0000000000001406

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183799/
https://www.ncbi.nlm.nih.gov/pubmed/34075901
http://dx.doi.org/10.1097/CM9.0000000000001406

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