Lv11
29 积分 2021-02-09 加入
Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation
2小时前
已完结
Variants leading to ELAVL2 haploinsufficiency cause a neurodevelopmental disorder with prominent cognitive, behavioral, and neurological features
8天前
已完结
A pilot study on collective effects of 22q13.31 deletions on gray matter concentration in schizophrenia
26天前
已完结
Clinical and molecular characterization of an emerging chromosome 22q13.31 microdeletion syndrome
26天前
已完结
Bi-allelic loss-of-function variants in TMEM63B cause syndromic surfactant dysfunction disorder
1个月前
已完结
Machine learning tool for predicting mature oocyte yield and trigger day from start of stimulation: towards personalized treatment
1个月前
已完结
The genetic architecture of morphological abnormalities of the sperm tail
2个月前
已完结
From whole-body to organ-specific biological age clocks
2个月前
已完结
Proteomic aging clocks in epidemiological studies: advances, applications and prospects
2个月前
已完结
Multimodal clocks of human aging
3个月前
已完结
Complications of Chemotherapy
10个月前
已采纳
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