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喵喵
Lv4
650 积分
2021-07-20 加入
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Steroid profile in dried blood spots by liquid chromatography tandem mass spectrometry: Application to newborn screening for congenital adrenal hyperplasia in China
7个月前
已完结
Novel human pathological mutations. Gene symbol: CYP17A1. Disease: 17alpha-hydroxylase/17,20-lyase deficiency
10个月前
已关闭
Molecular analysis of 12 Chinese patients with 11β‐hydroxylase deficiency and in vitro functional study of 20 CYP11B1 missense variants
11个月前
已完结
Clinical, pathophysiologic, genetic and therapeutic progress in Primary Bilateral Macronodular Adrenal Hyperplasia
11个月前
已完结
Molecular analysis of 12 Chinese patients with 11β‐hydroxylase deficiency and in vitro functional study of 20 CYP11B1 missense variants
1年前
已完结
Novel human pathological mutations. Gene symbol: CYP17A1. Disease: 17-alpha-hydroxylase/17,20-lyase deficiency
1年前
已关闭
A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency
1年前
已完结
Genetic analysis and novel variation identification in Chinese patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
1年前
已完结
Normal and Premature Adrenarche
1年前
已完结
Impact of Morphology in the Genotype and Phenotype Correlation of Bilateral Macronodular Adrenocortical Disease (BMAD): A Series of Clinicopathologically Well-Characterized 35 Cases
1年前
已完结
没有进行任何应助
速度真快
11个月前
来自ncbi【积分已退回】
1年前
速度真快,帮大忙了,点赞,感谢
1年前
求助的文献标题为: A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency,发表于1990年,上传的文献标题为:Missense mutation in CYP11B1 (CGA[Arg-384]→GGA[Gly]) causes steroid 11β-hydroxylase deficiency,发表于1995年
1年前
求助的文献标题为: A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency,发表于1990年 但上传的文献标题为:Missense mutation in CYP11B1 (CGA[Arg-384]→GGA[Gly]) causes steroid 11β-hydroxylase deficiency,发表于1995年
1年前
需要补充材料,不是正文
1年前
速度真快,帮大忙了
1年前
速度真快,帮大忙了,么么哒
1年前
点赞,感谢
1年前
速度真快,帮大忙了,点赞
1年前
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