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GABA Signaling Pathway-associated Gene PLCL1 Rare Variants May be Associated with Autism Spectrum Di
[期刊论文] 作者：Fengyun Zheng,Guoyuan Liu,Ting Dang,Qiaowen Chen,Yu An,Meng Wu,Xiangxuan Kong,Zilong Qiu,Bai-Lin Wu,
来源：神经科学通报（英文版） 年份：2021
Dear Editor,rnAutism spectrum disorders (ASDs) are neurodevelopmen-tal disorders with phenotypic and genetic heterogeneity,and are among the most heritable of neurodevelopmental disorders[1].Rare single nucleotide variants (SNVs) of genes a......
Characteristic face:A key indicator for direct diagnosis of 22q11.2 deletions in Chinese velocardiof
[会议论文] 作者：Dandan Wu,Guomin Wang,Yang Chen,Chen Xu,Ke Wang,Huijun Wang,Fengyun Zheng,Wantao Chen,Duan Ma,
来源：中华医学会2012年医学遗传学年会暨全国第十一次医学遗传学学术会议 年份：2012
Velocardiofacial syndrome(VCFS)is a disease in human with multiple anomalies,an expansive phenotypic spectrum,and diverse genetic mechanisms of copy number variations(CNVs)on 22qi 1.2 or other chromos...
[会议论文] 作者：Ping Zhang,Gendong Yao,Ma Duan,Chen Long,Huijun Wang,Shouxia Li,Ke Wang,Jin Zhang,Xinran Dong,Fengyun Zheng,
来源：第十二次全国医学遗传学学术会议 年份：2013
Background MicroRNAs (miRNAs) play an important role in organ development and may be factors in congenital malformations.The causes of non-syndromic, isolated cleft palate (NSCP) are still unclear; th...
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