Lv11
45 积分 2021-02-09 加入
Overlapping Xp21.2 duplications define an X-linked hypotrichosis simplex and implicate TAB3 dosage sensitivity
5小时前
待确认
Multi-omics analysis reveals fluorinated liquid crystal monomers BDPrB/EDPrB exposure disrupts the steroid biosynthesis function via inhibition of CYP17A1
1个月前
已完结
A pannexin 1 channelopathy causes human oocyte death
1个月前
已完结
Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation
1个月前
已完结
Variants leading to ELAVL2 haploinsufficiency cause a neurodevelopmental disorder with prominent cognitive, behavioral, and neurological features
1个月前
已完结
A pilot study on collective effects of 22q13.31 deletions on gray matter concentration in schizophrenia
2个月前
已完结
Clinical and molecular characterization of an emerging chromosome 22q13.31 microdeletion syndrome
2个月前
已完结
Bi-allelic loss-of-function variants in TMEM63B cause syndromic surfactant dysfunction disorder
2个月前
已完结
Machine learning tool for predicting mature oocyte yield and trigger day from start of stimulation: towards personalized treatment
3个月前
已完结
The genetic architecture of morphological abnormalities of the sperm tail
3个月前
已完结
Complications of Chemotherapy
1年前
已采纳
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