Lv13
90 积分 2025-01-23 加入
Pseudohypoparathyroidism: one gene, several syndromes
1小时前
已完结
Clinical Evaluation and Molecular Analysis of Genetic and Epigenetic Inactivation Defects in GNAS in children: A multicenter experience in China
2天前
已完结
Primary Invasive Cutaneous Fusariosis in Patients with STAT3 Hyper-IgE Syndrome
1个月前
已完结
Recessive Inheritance of Population-Specific Intronic LINE-1 Insertion Causes a Rotor Syndrome Phenotype
1个月前
已完结
Modes of Notch signalling in development and disease
1个月前
已完结
Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6
1个月前
已完结
Regulation of Tbx6 expression by Notch signaling
1个月前
已完结
Mendelian inheritance revisited: dominance and recessiveness in medical genetics
1个月前
已完结
Coronary artery disease and cardiovascular outcomes in patients with non-alcoholic fatty liver disease
2个月前
已完结
The Roles of T-Box Genes in Vertebrate Limb Development
2个月前
已完结
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