Coarctation of the aorta and mild to moderate developmental delay in a child with a de novo deletion of chromosome 15(q21.1q22.2)
一名患有主动脉缩窄和轻度至中度发育迟缓的儿童,其染色体 15(q21.1q22.2) 发生新生缺失。
期刊:BMC Medical Genetics
影响因子:
doi:10.1186/1471-2350-7-8
Lalani, Seema R; Sahoo, Trilochan; Sanders, Merideth E; Peters, Sarika U; Bejjani, Bassem A