Lv11
90 积分 2021-10-14 加入
Use of medical exome sequencing for identification of underlying genetic defects in NICU: Experience in a cohort of 2303 neonates in China
3小时前
已完结
A Child With Mild X-Linked Intellectual Disability and a Microduplication at Xp22.12 Including RPS6KA3
9天前
已完结
未破裂卵泡黄素化综合征患者伴X染色体异常一例
1个月前
已完结
A familial deletion of 10p12.1 associated with thrombocytopenia
1个月前
已完结
SRY基因阳性46,XX男性性反转综合征1例
1个月前
已完结
[Phenotypic and genotypic analysis of a girl carrying a 2q22.3 microduplication encompassing the MBD5 gene]
1个月前
已完结
A SOX3 duplication and lumbosacral spina bifida in three generations
2个月前
已完结
High frequency of genetic/epigenetic disorders in short stature children born with very low birth weight
2个月前
已完结
Critical prenatal diagnosis and management of incidental exon 43–44 deletion in the dystrophin gene
2个月前
已完结
The p.W651fsX666 mutation on COL10A1 results in impaired trimerization of normal collagen X to induce Schmid type Metaphyseal chondrodysplasia
2个月前
已关闭
Metal-Free Synthesis of Unsymmetrical Ureas and Carbamates from CO2 and Amines via Isocyanate Intermediates
11个月前
已采纳
Clinical and genetic features of retinoschisis in 120 families withRS1mutations
11个月前
已驳回
An integrated approach for line balancing and AGV scheduling towards smart assembly systems
11个月前
已采纳
六方氮化硼纳米颗粒增强生物聚合物纳米复合材料的结构，形态和介电性能
11个月前
已采纳
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