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
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author Zhang, Honghong
Sun, Yixi
Zhu, Yuxia
Hong, Jiali
Zheng, Miaomiao
author_facet Zhang, Honghong
Sun, Yixi
Zhu, Yuxia
Hong, Jiali
Zheng, Miaomiao
author_sort Zhang, Honghong
collection PubMed
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spelling pubmed-90491182022-04-29 Corrigendum: Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product Zhang, Honghong Sun, Yixi Zhu, Yuxia Hong, Jiali Zheng, Miaomiao Front Pediatr Pediatrics Frontiers Media S.A. 2022-04-14 /pmc/articles/PMC9049118/ /pubmed/35498794 http://dx.doi.org/10.3389/fped.2022.823860 Text en Copyright © 2022 Zhang, Sun, Zhu, Hong and Zheng. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Zhang, Honghong
Sun, Yixi
Zhu, Yuxia
Hong, Jiali
Zheng, Miaomiao
Corrigendum: Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product
title Corrigendum: Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product
title_full Corrigendum: Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product
title_fullStr Corrigendum: Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product
title_full_unstemmed Corrigendum: Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product
title_short Corrigendum: Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product
title_sort corrigendum: case report: prenatal diagnosis for a rett syndrome family caused by a novel mecp2 deletion with heteroduplexes of pcr product
topic Pediatrics
url 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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