P707: Additional evidence supporting and expanding the phenotype associated with MED12L loss-of-function variants
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2024-01-01
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| Series: | Genetics in Medicine Open |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S294977442400757X |
| _version_ | 1797267427110682624 |
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| author | Kristen Rasmussen Cassandra Runke Sarah Barnett Hutton Kearney Erik Thorland |
| author_facet | Kristen Rasmussen Cassandra Runke Sarah Barnett Hutton Kearney Erik Thorland |
| author_sort | Kristen Rasmussen |
| collection | DOAJ |
| first_indexed | 2024-04-25T01:16:24Z |
| format | Article |
| id | doaj.art-f250eb6f021543cfa90ef1ae0fd501d5 |
| institution | Directory Open Access Journal |
| issn | 2949-7744 |
| language | English |
| last_indexed | 2024-04-25T01:16:24Z |
| publishDate | 2024-01-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Genetics in Medicine Open |
| spelling | doaj.art-f250eb6f021543cfa90ef1ae0fd501d52024-03-09T09:33:18ZengElsevierGenetics in Medicine Open2949-77442024-01-012101611P707: Additional evidence supporting and expanding the phenotype associated with MED12L loss-of-function variantsKristen Rasmussen0Cassandra Runke1Sarah Barnett2Hutton Kearney3Erik Thorland4Division of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester MNDivision of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester MNDivision of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester MNDivision of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester MNDivision of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester MNhttp://www.sciencedirect.com/science/article/pii/S294977442400757X |
| spellingShingle | Kristen Rasmussen Cassandra Runke Sarah Barnett Hutton Kearney Erik Thorland P707: Additional evidence supporting and expanding the phenotype associated with MED12L loss-of-function variants Genetics in Medicine Open |
| title | P707: Additional evidence supporting and expanding the phenotype associated with MED12L loss-of-function variants |
| title_full | P707: Additional evidence supporting and expanding the phenotype associated with MED12L loss-of-function variants |
| title_fullStr | P707: Additional evidence supporting and expanding the phenotype associated with MED12L loss-of-function variants |
| title_full_unstemmed | P707: Additional evidence supporting and expanding the phenotype associated with MED12L loss-of-function variants |
| title_short | P707: Additional evidence supporting and expanding the phenotype associated with MED12L loss-of-function variants |
| title_sort | p707 additional evidence supporting and expanding the phenotype associated with med12l loss of function variants |
| url | http://www.sciencedirect.com/science/article/pii/S294977442400757X |
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