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1090 积分 2022-04-23 加入
CYP17A1 Pathogenic Variants in 26 Chinese Patients With 17α-Hydroxylase Deficiency by Targeted Long-Read Sequencing
4小时前
已完结
Growth hormone (GH) receptor knockout mice reveal actions of GH in lung development
2个月前
已完结
Mutations in MAP3K1 tilt the balance from SOX9/FGF9 to WNT/β-catenin signaling
3个月前
已完结
One case of congenital myopathy caused by new mutation of RYR1 gene and literature review
3个月前
已完结
Rapidly screening variants of uncertain significance in the MAP3K1 gene for phenotypic effects
5个月前
已完结
MAP3K1 functionally interacts with Axin1 in the canonical Wnt signalling pathway
5个月前
已完结
Biallelic mutations in FLNB cause a skeletal dysplasia with 46,XY gonadal dysgenesis by activating β-catenin
5个月前
已完结
46,XY disorders of sex development: the use of NGS for prevalent variants
5个月前
已完结
Whole exome sequencing applied to 42 Han Chinese patients with posterior hypospadias
5个月前
已完结
CYP17A1 Pathogenic Variants in 26 Chinese Patients with 17α-Hydroxylase Deficiency by Targeted Long-read Sequencing
6个月前
已完结
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