Froster-Iskenius U, Coerdt W, Rehder H, Schwinger E
Clin Genet. 1984 Dec;26(6):549-54. doi: 10.1111/j.1399-0004.1984.tb01102.x.
Cytogenetic and morphological findings of a 20-gestational-week-old female fetus with karyotype 46,XX,i(18q) are reported. The fetus displayed clinical features resembling Edward's syndrome. No characteristic symptoms of monosomy 18p could be observed.
报告了一名孕20周、核型为46,XX,i(18q)的女性胎儿的细胞遗传学和形态学检查结果。该胎儿表现出类似爱德华兹综合征的临床特征。未观察到18p单体的特征性症状。