de Grouchy J, Turleau C
U. 173 INSERM Hôpital Necker-Enfants-Malodes, Paris.
Recenti Prog Med. 1990 May;81(5):337-43.
The development of cytogenetic high resolution banding techniques has allowed the observation of specific chromosome rearrangements--i.e. microdeletions, translocations--in patients with morbid conditions suspected to have a genetic component but for which a precise etiology had not, or rarely, been recognized. The most striking examples are retinoblastoma, the WAGR complex, Beckwith-Wiedemann syndrome, Langer-Giedion syndrome, Prader-Willi syndrome, Miller-Dieker syndrome and others, which thus could be mapped to the genome. Molecular technology further allowed in a number of cases cloning of the genes proper or of linked DNA polymorphisms permitting genetic counseling.
细胞遗传学高分辨率显带技术的发展,使得在疑似有遗传因素但尚未或很少识别出确切病因的病态患者中,能够观察到特定的染色体重排,即微缺失、易位。最典型的例子是视网膜母细胞瘤、WAGR综合征、贝克威思-维德曼综合征、朗格-吉迪恩综合征、普拉德-威利综合征、米勒-迪克尔综合征等,因此可以将这些疾病定位到基因组中。分子技术在许多情况下进一步实现了相关基因或连锁DNA多态性的克隆,从而为遗传咨询提供了可能。