Maternally inherited unbalanced translocation of chromosome 22 in a 5-day-old neonate with persistent fifth aortic arch and tetralogy of Fallot [5]

Lee M.-L.Tsao L.-Y.Wang B.-T.Lee M.-H.ING-SH CHIU2020-03-122020-03-1220030167-5273https://www.scopus.com/inward/record.uri?eid=2-s2.0-0042384436&doi=10.1016%2fS0167-5273%2802%2900560-0&partnerID=40&md5=cccd969378085209c678b28f8776e4aahttps://scholars.lib.ntu.edu.tw/handle/123456789/475666[SDGs]SDG3prostaglandin E2; angiocardiography; aorta arch; case report; chromosome high resolution banding analysis; chromosome translocation 22; clinical feature; diagnostic imaging; disease course; Doppler echocardiography; extrachromosomal inheritance; Fallot tetralogy; female; fluorescence in situ hybridization; genetic counseling; heart catheterization; human; letter; lung atresia; medical examination; newborn; newborn intensive care; priority journal; treatment failureMaternally inherited unbalanced translocation of chromosome 22 in a 5-day-old neonate with persistent fifth aortic arch and tetralogy of Fallot [5]letter10.1016/S0167-5273(02)00560-0129577742-s2.0-0042384436