Lv3
290 积分 2022-12-16 加入
Novel MAP1B loss-of-function variant associated with periventricular nodular heterotopia 9 and literature review on genotype-phenotype associations of MAP1B
20小时前
已完结
Novel MAP1B loss-of-function variant associated with periventricular nodular heterotopia 9 and literature review on genotype-phenotype associations of MAP1B
20小时前
已完结
Sex, Age, and Gene
28天前
已完结
Filamin C in cardiomyopathy: from physiological roles to DNA variants
2个月前
已关闭
Genetic profile and genotype–phenotype correlations in childhood cardiomyopathy
7个月前
已完结
Variant sub-tiering, disease-gene associations and strictness of clinical criteria improves the interpretation of variants of uncertain significance in hereditary cardiomyopathies and rhythm disorders
7个月前
已关闭
Domain-specific association of single-nucleotide variants in the LMNA gene with the phenotypic expression of dilated cardiomyopathy
9个月前
已完结
Prevention of cancer therapy-related cardiac dysfunction and heart failure in cancer patients and survivors. A Clinical Consensus Statement of the Heart Failure Association, the European Association of Preventive Cardiology of the ESC, and the ESC Council of Cardio-Oncology
10个月前
已完结
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