Associated Papers
Clinical and Genetic Analysis of CHD7 Expands the Genotype and Phenotype of CHARGE Syndrome.
Qin Z et al.
Frontiers in Genetics, 2020
32625235 (PubMed )
Supplement: Data_Sheet_1.zip › Supplementary_Table_1.XLSX › P_or_LP_variants
Endocrinological Characteristics of 25 Japanese Patients with CHARGE Syndrome.
Shoji Y et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology, 2014
Phenotypic spectrum of CHARGE syndrome with CHD7 mutations.
Aramaki M et al.
The Journal of Pediatrics, 2006
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