Publications

Export 2 results:
Author Title [ Year(Asc)]
Filters: Keyword is Embryonic Development  [Clear All Filters]
2020
Beck, D. B. et al. Delineation of a Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 Deficiency. Am J Hum Genet 106, 234-245 (2020).
2017
Liu, P. et al. An Organismal CNV Mutator Phenotype Restricted to Early Human Development. Cell 168, 830-842.e7 (2017).