Lv6
2230 积分 2020-06-03 加入
De Novo Mutated TUBB2B Associated Pachygyria Diagnosed by Medical Exome Sequencing and Long-Range PCR
1个月前
已完结
IncreasedSTAG2dosage defines a novel cohesinopathy with intellectual disability and behavioral problems
1个月前
已完结
IncreasedSTAG2dosage defines a novel cohesinopathy with intellectual disability and behavioral problems
1个月前
已完结
Imprinting disorders
2个月前
已完结
Mendelian randomization analysis reveals causal associations between autoimmune diseases and female infertility risk
5个月前
已完结
Genetic evidence linking retinol to birth weight: A two-sample Mendelian randomization study
5个月前
已关闭
Maternal hypertensive disorders of pregnancy and childhood neurodevelopmental disorders: A two‐sample Mendelian randomization
5个月前
已完结
Perinatal prevalence of birth defects in the Mainland of China, 2000–2021: a systematic review and meta-analysis
7个月前
已完结
Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling
7个月前
已关闭
Prenatal genetic investigation in pregnancies with oligohydramnios: Results from a single referral medical center
7个月前
已完结
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