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76 积分 2025-04-12 加入
A novel mutation in the FOXC1 gene in a family with Axenfeld-Rieger syndrome and Peters' anomaly
21小时前
待确认
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
12天前
已完结
Comparison of Bioinformatics Prediction, Molecular Modeling, and Functional Analyses of FOXC1 Mutations in Patients with Axenfeld‐Rieger Syndrome
1个月前
已完结
Sibs with growth deficiency, delayed bone age, congenital hip dislocation, and iridocorneal abnormalities with glaucoma
1个月前
已完结
Axenfeld‐Rieger syndrome
2个月前
已完结
Integrating clinical and genetic insights in anterior segment dysgenesis with glaucoma: A contemporary review
2个月前
已完结
Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld–Rieger syndrome and glaucoma
3个月前
已完结
STIM1 in-frame deletion of eight amino acids in a patient with moderate tubular aggregate myopathy/Stormorken syndrome
3个月前
已关闭
Comparison of Bioinformatics Prediction, Molecular Modeling, and Functional Analyses ofFOXC1Mutations in Patients with Axenfeld-Rieger Syndrome
3个月前
已完结
Identification of genes involved in glaucoma pathogenesis using combined network analysis and empirical studies
3个月前
已完结
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