Copy number variation in patients with disorders of sex development due to 46,XY gonadal dysgenesis.
第一作者:
Stefan,White
第一单位:
Murdoch Childrens Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.
作者:
主题词
算法(Algorithms);动物(Animals);钙-钙调素依赖性蛋白激酶1型(Calcium-Calmodulin-Dependent Protein Kinase Type 1);染色体畸变(Chromosome Aberrations);染色体缺失(Chromosome Deletion);染色体, 人, 17对(Chromosomes, Human, Pair 17);染色体, 人, 8对(Chromosomes, Human, Pair 8);DNA拷贝数变异(DNA Copy Number Variations);女(雌)性(Female);GATA4转录因子(GATA4 Transcription Factor);基因表达调控(Gene Expression Regulation);基因重排(Gene Rearrangement);性腺发育不全, 46,XY(Gonadal Dysgenesis, 46,XY);性腺(Gonads);HSP40热休克蛋白质类(HSP40 Heat-Shock Proteins);人类(Humans);男(雄)性(Male);小鼠(Mice);寡核苷酸序列分析(Oligonucleotide Array Sequence Analysis);SOX9转录因子类(SOX9 Transcription Factor)
DOI
10.1371/journal.pone.0017793
PMID
21408189
发布时间
2024-11-01
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