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Dataset - Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
Details
Dataset - Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
Date Issued
2020
Author(s)
REPETTO LISBOA, MARIA GABRIELA
Facultad de Medicina Clínica Alemana Universidad del Desarrollo
Publication(s)
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome