P301: Incidental finding of MECP2-related disorder in a male infant with chromosome 15q11.2 microdeletion (Burnside–Butler) syndrome
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2023-01-01
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| Series: | Genetics in Medicine Open |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2949774423003291 |
| _version_ | 1797342010866139136 |
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| author | Zohra Shad Prisca Mbonu Kelly Pagidas |
| author_facet | Zohra Shad Prisca Mbonu Kelly Pagidas |
| author_sort | Zohra Shad |
| collection | DOAJ |
| first_indexed | 2024-03-08T10:27:15Z |
| format | Article |
| id | doaj.art-1449f9e9587d47cabc22172fd89f613e |
| institution | Directory Open Access Journal |
| issn | 2949-7744 |
| language | English |
| last_indexed | 2024-03-08T10:27:15Z |
| publishDate | 2023-01-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Genetics in Medicine Open |
| spelling | doaj.art-1449f9e9587d47cabc22172fd89f613e2024-01-27T07:07:36ZengElsevierGenetics in Medicine Open2949-77442023-01-0111100329P301: Incidental finding of MECP2-related disorder in a male infant with chromosome 15q11.2 microdeletion (Burnside–Butler) syndromeZohra Shad0Prisca Mbonu1Kelly Pagidas2Anne Burnett Marion School of Medicine at TCU, Fort Worth, TXAnne Burnett Marion School of Medicine at TCU, Fort Worth, TXAnne Burnett Marion School of Medicine at TCU, Fort Worth, TXhttp://www.sciencedirect.com/science/article/pii/S2949774423003291 |
| spellingShingle | Zohra Shad Prisca Mbonu Kelly Pagidas P301: Incidental finding of MECP2-related disorder in a male infant with chromosome 15q11.2 microdeletion (Burnside–Butler) syndrome Genetics in Medicine Open |
| title | P301: Incidental finding of MECP2-related disorder in a male infant with chromosome 15q11.2 microdeletion (Burnside–Butler) syndrome |
| title_full | P301: Incidental finding of MECP2-related disorder in a male infant with chromosome 15q11.2 microdeletion (Burnside–Butler) syndrome |
| title_fullStr | P301: Incidental finding of MECP2-related disorder in a male infant with chromosome 15q11.2 microdeletion (Burnside–Butler) syndrome |
| title_full_unstemmed | P301: Incidental finding of MECP2-related disorder in a male infant with chromosome 15q11.2 microdeletion (Burnside–Butler) syndrome |
| title_short | P301: Incidental finding of MECP2-related disorder in a male infant with chromosome 15q11.2 microdeletion (Burnside–Butler) syndrome |
| title_sort | p301 incidental finding of mecp2 related disorder in a male infant with chromosome 15q11 2 microdeletion burnside butler syndrome |
| url | http://www.sciencedirect.com/science/article/pii/S2949774423003291 |
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