Associated Papers
Investigating USP42 Mutation as Underlying Cause of Familial Non-Medullary Thyroid Carcinoma.
Teixeira E et al.
International Journal of Molecular Sciences, 2024
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_2.XLSX › patient_3
Select a paper to view details