Lv1
20 积分 2022-05-06 加入
Clinical utility of comprehensive gene panel testing for common and rare causes of skeletal dysplasia and other skeletal disorders: Results from the largest cohort to date
2个月前
已完结
Genotypic and phenotypic analysis of Korean patients with tuberous sclerosis complex
2个月前
已完结
Tuberous sclerosis complex: Clinical, genetic and 7T-MRI neuroimaging findings
2个月前
已完结
Genotypic and phenotypic analysis of Korean patients with tuberous sclerosis complex
2个月前
已完结
Combination of Radiotherapy and Immunotherapy in Advanced Non–Small Cell Lung Cancer
2个月前
已完结
Intellectual disability and abnormal cortical neuron phenotypes in patients with Bloom syndrome
2个月前
已完结
Long-term observation of patients with advanced late-onset Pompe disease undergoing enzyme replacement therapy: A 15-year observation in a single center
2个月前
已完结
Oncologist-led germline genetic testing for uveal melanoma
7个月前
已完结
Oncologist-led germline genetic testing for uveal melanoma
7个月前
已完结
Novel de novo mutation in KAT6A gene in a child with severe aplastic anemia
7个月前
已完结
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