Analysis of genotype-phenotype correlations in human holoprosencephaly.

导出 OA

翻译打印收藏纠错

作者： Benjamin D,Solomon ^[1] ; Sandra,Mercier ; Jorge I,Vélez ; Daniel E,Pineda-Alvarez ; Adrian,Wyllie ; Nan,Zhou ; Christèle,Dubourg ; Veronique,David ; Sylvie,Odent ; Erich,Roessler ; Maximilian,Muenke

作者单位： National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA. ^[1]

主题词动物(Animals);DNA突变分析(DNA Mutational Analysis);基因型(Genotype);猬蛋白质类(Hedgehog Proteins);前脑无裂畸形(Holoprosencephaly);人类(Humans);核蛋白质类(Nuclear Proteins);表型(Phenotype);转录因子(Transcription Factors)

DOI 10.1002/ajmg.c.30240

PMID 20104608

发布时间 2022-04-09

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交

浏览33

American journal of medical genetics. Part C, Seminars in medical genetics

2010年154C卷1期

133-41页

相似文献

中文期刊
外文期刊
学位论文
会议论文

检索历史清除

Analysis of genotype-phenotype correlations in human holoprosencephaly.

American journal of medical genetics. Part C, Seminars in medical genetics

相似文献

American journal of medical genetics. Part C, Seminars in medical genetics

相关期刊

参考文献：
指定格式：	NoteExpress EndNote RefWorks NoteFirst

检索历史 清除

Analysis of genotype-phenotype correlations in human holoprosencephaly.

American journal of medical genetics. Part C, Seminars in medical genetics

相似文献

American journal of medical genetics. Part C, Seminars in medical genetics

相关期刊

检索历史清除