Publications
Export 1 results:
Author Title [ Year
] Filters: Keyword is Infant, Newborn and Author is Arts, Peer [Clear All Filters]
Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1-related syndrome. Am J Med Genet A 182, 1273-1277 (2020).
