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. |
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| 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 |
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