换一批
换一批Reduced penetrance of craniofacial anomalies as a function of deletion size and genetic background in a chromosome engineered partial mouse model for Smith-Magenis syndrome.
第一作者：
Jiong,Yan
第一单位：
Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA.
作者：
主题词
畸形, 多发性(Abnormalities, Multiple);动物(Animals);细胞, 培养的(Cells, Cultured);染色体图(Chromosome Mapping);染色体, 人, 17对(Chromosomes, Human, Pair 17);颅面骨畸形(Craniofacial Abnormalities);疾病模型, 动物(Disease Models, Animal);基因缺失(Gene Deletion);遗传工程(Genetic Engineering);遗传变异(Genetic Variation);遗传载体(Genetic Vectors);基因组(Genome);杂合子(Heterozygote);人类(Humans);原位杂交, 荧光(In Situ Hybridization, Fluorescence);小鼠(Mice);小鼠, 近交C57BL(Mice, Inbred C57BL);小鼠, 突变型(Mice, Mutant Strains);外显率(Penetrance);逆转录病毒科(Retroviridae);干细胞(Stem Cells);综合征(Syndrome);同线性(Synteny)
DOI
10.1093/hmg/ddh288
PMID
15459175
发布时间
2008-11-21
- 浏览4
Human molecular genetics
2613-24页
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