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Maternal Xp22.31 copy-number variations detected in non-invasive prenatal screening effectively guide the prenatal diagnosis of X-linked ichthyosis.

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Title: Maternal Xp22.31 copy-number variations detected in non-invasive prenatal screening effectively guide the prenatal diagnosis of X-linked ichthyosis.
Authors: Tang X; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, China., Wang Z; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, China., Yang S; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, China., Chen M; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, China., Zhang Y; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, China., Zhang F; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, China., Tan J; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, China., Yin T; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, China., Wang L; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, China.
Source: Frontiers in genetics [Front Genet] 2022 Aug 31; Vol. 13, pp. 934952. Date of Electronic Publication: 2022 Aug 31 (Print Publication: 2022).
Publication Type: Journal Article
Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1664-8021
DOI:10.3389/fgene.2022.934952