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Editorial: Fetal phenotypes of rare diseases: application and evaluation of prenatal exome sequencing and pathogenesis research of rare diseases
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10204703/ https://www.ncbi.nlm.nih.gov/pubmed/37229199 http://dx.doi.org/10.3389/fgene.2023.1205726 |
| _version_ | 1785045889053622272 |
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| author | Zhang, Yan Ding, Can Chen, Yiwei Wu, Meng Luo, Min |
| author_facet | Zhang, Yan Ding, Can Chen, Yiwei Wu, Meng Luo, Min |
| author_sort | Zhang, Yan |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-10204703 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2023 |
| publisher | Frontiers Media S.A. |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-102047032023-05-24 Editorial: Fetal phenotypes of rare diseases: application and evaluation of prenatal exome sequencing and pathogenesis research of rare diseases Zhang, Yan Ding, Can Chen, Yiwei Wu, Meng Luo, Min Front Genet Genetics Frontiers Media S.A. 2023-05-09 /pmc/articles/PMC10204703/ /pubmed/37229199 http://dx.doi.org/10.3389/fgene.2023.1205726 Text en Copyright © 2023 Zhang, Ding, Chen, Wu and Luo. 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 | Genetics Zhang, Yan Ding, Can Chen, Yiwei Wu, Meng Luo, Min Editorial: Fetal phenotypes of rare diseases: application and evaluation of prenatal exome sequencing and pathogenesis research of rare diseases |
| title | Editorial: Fetal phenotypes of rare diseases: application and evaluation of prenatal exome sequencing and pathogenesis research of rare diseases |
| title_full | Editorial: Fetal phenotypes of rare diseases: application and evaluation of prenatal exome sequencing and pathogenesis research of rare diseases |
| title_fullStr | Editorial: Fetal phenotypes of rare diseases: application and evaluation of prenatal exome sequencing and pathogenesis research of rare diseases |
| title_full_unstemmed | Editorial: Fetal phenotypes of rare diseases: application and evaluation of prenatal exome sequencing and pathogenesis research of rare diseases |
| title_short | Editorial: Fetal phenotypes of rare diseases: application and evaluation of prenatal exome sequencing and pathogenesis research of rare diseases |
| title_sort | editorial: fetal phenotypes of rare diseases: application and evaluation of prenatal exome sequencing and pathogenesis research of rare diseases |
| topic | Genetics |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10204703/ https://www.ncbi.nlm.nih.gov/pubmed/37229199 http://dx.doi.org/10.3389/fgene.2023.1205726 |
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