Associated Papers
Classification of CHD7 Rare Variants in Chinese Congenital Hypogonadotropic Hypogonadism Patients and Analysis of Their Clinical Characteristics.
Sun B et al.
Frontiers in Genetics, 2021
Evaluating systematic reanalysis of clinical genomic data in rare disease from single center experience and literature review.
Tan NB et al.
Molecular Genetics & Genomic Medicine, 2020
Phenotypic spectrum of CHARGE syndrome with CHD7 mutations.
Aramaki M et al.
The Journal of Pediatrics, 2006
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