Genetic architecture of laterality defects revealed by whole exome sequencing - Li, Alexander H.; Hanchard, Neil A.; Azamian, Mahshid; D’Alessandro, Lisa C. A.; Coban-Akdemir, Zeynep; Lopez, Keila N.; Hall, Nancy J.; Dickerson, Heather; Nicosia, Annarita; Fernbach, Susan; Boone, Philip M.; Gambin, Tomaz; et al. (European journal of human genetics : EJHG, 2019)
Keywords: Congenital defects; Defects; Embryogenesis; Islet-1 protein; Phenotypes; Primary ciliary dyskinesia; Smad2 protein; Whole genome sequencing