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De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype.
- Source :
-
American Journal of Human Genetics . Jan2017, Vol. 100 Issue 1, p179-179. 1p. - Publication Year :
- 2017
- Subjects :
- *PHENOTYPES
Subjects
Details
- Language :
- English
- ISSN :
- 00029297
- Volume :
- 100
- Issue :
- 1
- Database :
- Academic Search Index
- Journal :
- American Journal of Human Genetics
- Publication Type :
- Academic Journal
- Accession number :
- 120517641
- Full Text :
- https://doi.org/10.1016/j.ajhg.2016.12.004