染色体10q24.31片段重复导致先天性缺指/缺趾畸形的一个家系致病机理分析

张秀泉,王建,熊符,吕伟标,周远青,杨少民,张玉婷,田小燕,连蔚,徐湘民

Congenital ectrodactyly caused by chromosome 10q24.31 duplication and its pathogenetic analysis

Zhang Xiuquan,Wang Jian,Xiong Fu,Lv Weibiao,Zhou Yuanqing,Yang Shaomin,Zhang Yuting,Tian Xiaoyan,Lian Wei,Xu Xiangmin

图1 SHFM患者家系图 该家系共调查了5代共有6例患者,男女都有发病,共有男性患者4例、女性患者2例。箭头指向先证者。

Fig. 1 Pedigree of the ectrodactyly family