Voullaire L E, Webb G C, Leversha M
Department of Genetics, Royal Children's Hospital, Parkville, Victoria, Australia.
J Med Genet. 1989 Jul;26(7):439-42. doi: 10.1136/jmg.26.7.439.
Chromosome results obtained from 1012 patients referred with developmental delay without known cause within the three years 1985 to 1987 are reported. G banding analysis and assessment of 70 cells for fragile X gave abnormal results in 84 cases: fragile X in 31 patients and other abnormalities in 53 patients. A further 16 sibs expressing the fragile X were detected in family studies originating from the 31 index cases. This yield justifies continuation of procedures which detect both fragile X and subtle chromosomal abnormalities in these patients.
报告了1985年至1987年这三年间,对1012名因发育迟缓前来就诊且病因不明的患者进行染色体检查的结果。通过G显带分析并对70个细胞进行脆性X评估,结果显示84例异常:31例患者为脆性X,53例患者为其他异常。在源于31例索引病例的家系研究中,又检测出16名表达脆性X的同胞。这一结果表明,继续采用能够检测这些患者脆性X和细微染色体异常的检测方法是合理的。