Lv41
650 积分 2022-03-06 加入
EpiTyping: analysis of epigenetic aberrations in parental imprinting and X-chromosome inactivation using RNA-seq
1个月前
已完结
Animal Models of Cerebral Palsy: What Can We Learn About Cerebral Palsy in Humans
4个月前
已完结
ADGRL1 haploinsufficiency causes a variable spectrum of neurodevelopmental disorders in humans and alters synaptic activity and behavior in a mouse model
5个月前
已完结
Azoospermia in patients heterozygous for a mutation in SYCP3
5个月前
已完结
Bi-allelic variants in chromatoid body protein TDRD6 cause spermiogenesis defects and severe oligoasthenoteratozoospermia in humans
5个月前
已完结
Skipping of exon 12 as a consequence of a point mutation (1898 + 5G → T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese family
8个月前
已关闭
Defective piRNA Processing and Azoospermia
11个月前
已完结
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype
1年前
已完结
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