Martín Sánchez A, Delicado A, Izquierdo M, Oliver A, López Pajares I, Gracia R, Peralta A
An Esp Pediatr. 1981 May;14(5):344-51.
Two cases of trisomy 9p, are reported affecting different break points involving chromosome 9; one of them showed skeletal abnormalities of importance. An analysis of the two cases reported is done and some of the last hypothesis in order to determine genetical and clinical correlations of the syndrome are considered.
报告了两例9号染色体短臂三体病例,涉及9号染色体的不同断点;其中一例表现出明显的骨骼异常。对报告的这两例病例进行了分析,并考虑了一些最新的假设,以确定该综合征的遗传和临床相关性。