A new embryologic linkage between chromosome 22q11 deletion and a right ductus from a right aortic arch in a neonate with DiGeorge syndrome [6]

Lee M.-L.Chaou W.-T.Wang Y.-M.Fang W.ING-SH CHIU2020-03-122020-03-1220010167-5273https://www.scopus.com/inward/record.uri?eid=2-s2.0-0034742768&doi=10.1016%2fS0167-5273%2801%2900431-4&partnerID=40&md5=1dfcb32d3da6f339501d3b00dc97b800https://scholars.lib.ntu.edu.tw/handle/123456789/475674[SDGs]SDG3calcitriol; gluconate calcium; magnesium sulfate; aorta arch; artery malformation; case report; cell migration; chromosome deletion; clinical feature; DiGeorge syndrome; disease association; ductus arteriosus; embryo pattern formation; face dysmorphia; human; hypocalcemia; hypoparathyroidism; intractable epilepsy; letter; male; neural crest cell; newborn; patent ductus arteriosus; phenotype; priority journal; chromosome 22; congenital heart malformation; congenital malformation; DiGeorge syndrome; gene deletion; genetics; patent ductus arteriosus; prenatal development; thoracic aorta; Aorta, Thoracic; Chromosomes, Human, Pair 22; DiGeorge Syndrome; Ductus Arteriosus, Patent; Gene Deletion; Heart Defects, Congenital; Humans; Infant, Newborn; MaleA new embryologic linkage between chromosome 22q11 deletion and a right ductus from a right aortic arch in a neonate with DiGeorge syndrome [6]letter10.1016/S0167-5273(01)00431-4114882862-s2.0-0034742768