Roberts syndrome and SC phocomelia. A single genetic entity
Roberts syndrome and SC phocomelia. A single genetic entity
复制标题
罗伯茨综合征和 SC 海虱病。
作者：
C. Römke;U. Froster;K. Heyne;W. Höhn;M. Hof;Grzegorz Grzetszczyk;R. Rauskolb;H. Rehder;E. Schwinger
一个家庭有三个兄弟姐妹表现出不同的表现罗伯茨综合征或SC短肢畸形的描述。关于以前发表的家族性罗伯茨综合征和SC短肢畸形的病例，我们得出结论，这两种综合征是同一个遗传实体。
A family with three siblings showing different manifestations of Roberts syndrome or SC phocomelia is described. With regard to previously published cases of familial Roberts syndrome and SC phocomelia we conclude that these two syndromes are one and the same genetic entity.
罗伯茨综合征成纤维细胞细胞分裂周期的异常：表型特征的细胞基础？
影响因子：
9.8
作者：
Tomkins,DJ;Sisken,JE
通讯作者：
Sisken,JE