Seabright M, Lewis G M
Hum Genet. 1978 Jun 9;42(2):223-6. doi: 10.1007/BF00283642.
Chromosome studies were carried out on three patients for the following reasons: (1) growth retardation and mental subnormality in a boy; (2) marked developmental delay in a female infant; (3) routine check on a man whose wife had a stillborn with congenital anomalies. An interstitial deletion at 7q11::7q21 was observed in all three cases.
出于以下原因,对三名患者进行了染色体研究:(1)一名男孩生长发育迟缓且智力低下;(2)一名女婴明显发育延迟;(3)对一名男子进行常规检查,其妻子曾有过一个患有先天性异常的死产儿。在所有三例中均观察到7号染色体长臂1区1带至7号染色体长臂2区1带的中间缺失。