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xiaominza
Lv1
3
90 积分
2024-03-29 加入
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Proteolipid protein 1 and gap junction α12 gene mutations in 72 Chinese patients with Pelizaeus-Merzbacher disease/ Pelizaeus-Merzbacher like disease and prenatal diagnosis of 15 fetuses in twelve Chinese families with PMD probands
1小时前
求助中
Targeted disruption of Otog results in deafness and severe imbalance
23小时前
已完结
[Clinical and genetic analysis of a family with Aicardi-Goutières syndrome and literature review]
4天前
已完结
Biochemical and pharmacogenetic dissection of human steroid 5??-reductase type II
14天前
已完结
Homozygous p.R246Q Mutation and Impaired Spermatogenesis: Long Term Follow-up of 4 Children from One Family with 5 Alpha Reductase 2 Deficiency
15天前
已完结
综合性携带者筛查关键问题专家共识(2024版)
17天前
已完结
Low prevalence of classical galactosemia in Korean population
22天前
已完结
FSIP2plays a role in the acrosome development during spermiogenesis
27天前
已完结
Ovarian insufficiency and secondary amenorrhea in a patient with a novel variant within GDF9 gene
28天前
已完结
BiallelicCFAP61variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia
28天前
已完结
没有进行任何应助
感谢,速度真快,么么哒
4天前
速度真快,感谢
14天前
感谢,帮大忙了
15天前
感谢,帮大忙了
16天前
感谢,点赞
22天前
感谢,速度真快,点赞
27天前
速度真快,感谢
1个月前
速度真快,感谢
1个月前
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