Shabtai F, Shalev A, Chemke J, Halbrecht I, Elian E
Hum Genet. 1979;52(3):263-8. doi: 10.1007/BF00278675.
A patient with pure trisomy of the short arm of chromosome 17 in 60% of the examined cells is reported. She presented a variant chromosome 1 with partial pericentric inversion and increased centromeric heterochromatin in one chromosome 17. The cytogenetic findings are discussed. The clinical findings are compared to those found in other reported cases of partial trisomy 17 and a delineation of a pure trisomy 17p attempted.
报告了一名患者,在60%的检测细胞中存在17号染色体短臂的纯三体性。她有一条变异的1号染色体,带有部分臂间倒位,且一条17号染色体上的着丝粒异染色质增加。对细胞遗传学发现进行了讨论。将临床发现与其他报道的部分17号染色体三体病例的发现进行了比较,并尝试对纯17号染色体短臂三体进行描述。