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The diagnosis of the first-documented intragenic KANSL1 microduplication patient broadens the genetic spectrum of Koolen de Vries syndrome.
- Source :
- Clinical Genetics; May/Jun2022, Vol. 101 Issue 5/6, p575-576, 2p
- Publication Year :
- 2022
Details
- Language :
- English
- ISSN :
- 00099163
- Volume :
- 101
- Issue :
- 5/6
- Database :
- Complementary Index
- Journal :
- Clinical Genetics
- Publication Type :
- Academic Journal
- Accession number :
- 157309223
- Full Text :
- https://doi.org/10.1111/cge.14124