Skip to Main Content

Paper Details

Clinical Syndromic Phenotypes and the Potential Role of Genetics in Pulmonary Vein Stenosis.
Children (Basel)
5
2021
CAVC, CHD, CLD, Children, PHTN, PVS, Pulmonary Vein Stenosis, Pulmonary vein stenosis, Smith-Lemli-Opitz Syndrome, T21, Trisomy 21, chronic lung disease, common atrioventricular canal, congenital heart disease, pathologic genetic disease, patients, prematurity, pulmonary hypertension, pulmonary venous obstruction, syndromic
Author NameAffiliation
Abbas Haider ZaidiBoston Children's Hospital
Abbas Haider ZaidiHarvard Medical School
Jessica M YamadaBoston Children's Hospital
David T MillerHarvard Medical School
David T MillerBoston Children's Hospital
Kerry McEnaneyBoston Children's Hospital
Christina IrelandBoston Children's Hospital
Amy E RobertsBoston Children's Hospital
Amy E RobertsBoston Children's Hospital
Amy E RobertsHarvard Medical School
Amy E RobertsBoston Children's Hospital
Amy E RobertsHarvard Medical School
Amy E RobertsBoston Children's Hospital
Kimberlee GauvreauBoston Children's Hospital
Kimberlee GauvreauHarvard Medical School
Kathy J JenkinsBoston Children's Hospital
Kathy J JenkinsHarvard Medical School
Ming-Hui ChenBoston Children's Hospital
Ming-Hui ChenHarvard Medical School
Ming-Hui ChenBoston Children's Hospital
  • 1 - 20

Datasets

Release 1.2