A familial GLI2 deletion (2q14.2) not associated with the holoprosencephaly syndrome phenotype: A familial GLI2 deletion (2q14.2)Lukas Soellner,Thomas Eggermann,Ulrike Kordas,Carmen Schroder,Miriam ElbrachtAmerican Journal of Medical Genetics Part A（2015）引用 37|浏览2暂无评分AI 理解论文溯源树样例生成溯源树，研究论文发展脉络Chat Paper正在生成论文摘要
