对22三体研究的一项新贡献。
A new contribution to the study of 22 trisomy.
作者信息
Pérez-Castillo A, Abrisqueta J A, Martin-Lucas M A, Goday C, Del Mazo J, Aller V
出版信息
Humangenetik. 1975 Sep 20;30(3):265-71. doi: 10.1007/BF00279192.
PMID:1184009
Abstract
The case of a 2 1/2-month-old male child with intrauterine distrophy features and multiple congenital malformations is presented. Cytogenetic studies of the child and his parents, completed with Q- and G-banding techniques led us to conclude that it is a case of 22 trisomy inherited from his mother.
摘要
本文报告了一例2个半月大的男婴，具有宫内发育不良特征及多种先天性畸形。运用Q带和G带技术对该患儿及其父母进行细胞遗传学研究后，我们得出结论，这是一例由其母亲遗传而来的22三体综合征病例。
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