Segmental uniparental disomy as a rare cause of congenital severe factor XIII deficiency in a girl with only one heterozygous carrier parent

MING-CHING SHENChen M.Chang S.-P.Lin P.-T.Hsieh H.-N.Lin K.-H.2021-05-252021-05-2520180888-0018https://scholars.lib.ntu.edu.tw/handle/123456789/562330Segmental uniparental disomy as a rare cause of congenital severe factor XIII deficiency in a girl with only one heterozygous carrier parentletter10.1080/08880018.2018.1546783307023812-s2.0-85060996496