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

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Bibliographic Details
Main Authors:	Honghong Zhang (Author), Yixi Sun (Author), Yuxia Zhu (Author), Jiali Hong (Author), Miaomiao Zheng (Author)
Format:	Book
Published:	Frontiers Media S.A., 2022-04-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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042			\|a dc
100	1	0	\|a Honghong Zhang \|e author
700	1	0	\|a Yixi Sun \|e author
700	1	0	\|a Yixi Sun \|e author
700	1	0	\|a Yuxia Zhu \|e author
700	1	0	\|a Jiali Hong \|e author
700	1	0	\|a Miaomiao Zheng \|e author
245	0	0	\|a Corrigendum: Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product
260			\|b Frontiers Media S.A., \|c 2022-04-01T00:00:00Z.
500			\|a 2296-2360
500			\|a 10.3389/fped.2022.823860
546			\|a EN
690			\|a Rett syndrome
690			\|a MECP2
690			\|a prenatal diagnosis
690			\|a mosaicism
690			\|a heteroduplexes
690			\|a Pediatrics
690			\|a RJ1-570
655	7		\|a article \|2 local
786	0		\|n Frontiers in Pediatrics, Vol 10 (2022)
787	0		\|n https://www.frontiersin.org/articles/10.3389/fped.2022.823860/full
787	0		\|n https://doaj.org/toc/2296-2360
856	4	1	\|u https://doaj.org/article/f45fd86083414623912d19f2e9da9bc6 \|z Connect to this object online.