Tomkins D J, Gitelman B J, Roberts M H
Hum Genet. 1983;63(4):369-73. doi: 10.1007/BF00274764.
A girl with mental retardation and the facies associated with the distal 10q duplication syndrome was found to have a tandem duplication of 10q24 to 10q26. This was confirmed by gene dosage studies of glutamic oxaloacetic transaminase 1. The clinical features of this patient are compared with those of other reported cases of the distal 10q duplication syndrome with duplication-deficiency karyotypes due to familial reciprocal translocations or inversions or with tandem duplication of a more proximal region of 10q. Reports of tandem duplications in man and possible mechanisms of origin are discussed.
一名患有智力障碍及与10q远端重复综合征相关面容的女孩,被发现存在10q24至10q26的串联重复。这通过谷氨酸草酰乙酸转氨酶1的基因剂量研究得以证实。将该患者的临床特征与其他报道的因家族性相互易位或倒位导致重复 - 缺失核型的10q远端重复综合征病例,或10q更近端区域串联重复的病例进行了比较。讨论了人类串联重复的报道及可能的起源机制。