Corrigendum: Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product

Detalles Bibliográficos
Autores principales: Zhang, Honghong, Sun, Yixi, Zhu, Yuxia, Hong, Jiali, Zheng, Miaomiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049118/
https://www.ncbi.nlm.nih.gov/pubmed/35498794
http://dx.doi.org/10.3389/fped.2022.823860

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049118/
https://www.ncbi.nlm.nih.gov/pubmed/35498794
http://dx.doi.org/10.3389/fped.2022.823860

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