Kumar D, Blank C E, Griffiths B L
J Med Genet. 1985 Aug;22(4):296-300. doi: 10.1136/jmg.22.4.296.
A family is reported in which several members have the Cornelia de Lange syndrome and other members show facial dysmorphism and other features reminiscent of this syndrome. The segregation pattern is consistent with the view that the dysmorphic features (variable) are the manifestation of a single gene in heterozygous form. Chromosome abnormality was not found.
据报道,有一个家族,其中几名成员患有科妮莉亚·德·朗热综合征,其他成员则表现出面部畸形及其他类似该综合征的特征。分离模式与以下观点一致,即这些畸形特征(可变)是杂合形式的单个基因的表现。未发现染色体异常。