Schmid M, Wolf J, Nestler H, Krone W
Hum Genet. 1979 Jul 18;49(3):283-9. doi: 10.1007/BF00569348.
A partial trisomy for the distal segment of the long arm of chromosome 7 (bands q32 replaced by qter) was observed in a severely retarded child with somatic and CNS anomalies. The phenotypically normal father and paternal grandmother had a balanced reciprocal translocation between the long arm of a chromosome 2 and the long arm of a chromosome 7: 46,XX-XY,t(2;7) (q37;q32). The clinical features of the child at birth and at the ages of 5 months and 2 years are compared with those previously reported in cases of partial trisomy 7q.
在一名患有躯体和中枢神经系统异常的严重智力发育迟缓儿童中,观察到7号染色体长臂远端片段(q32带被qter取代)的部分三体性。表型正常的父亲和祖母在2号染色体长臂与7号染色体长臂之间存在平衡易位:46,XX-XY,t(2;7)(q37;q32)。将该儿童出生时、5个月和2岁时的临床特征与先前报道的7q部分三体病例的特征进行了比较。