Congenital Heart Defects and Dysmorphic Facial Features in Patients Suspicious of 22q11.2 Deletion Syndrome in Southern Brazil
| Autor: | Diniz, Bruna Lixinski, Santos, Andressa Schneiders, Glaeser, Andressa Barreto, Guaraná, Bruna Baierle, Lorea, Cláudia Fernandes, Josahkian, Juliana Alves, Huber, Janaína, Rosa, Rafael Fabiano Machado, Zen, Paulo Ricardo Gazzola |
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| Zdroj: | Journal of Pediatric Genetics; December 2020, Vol. 9 Issue: 4 p227-234, 8p |
| Databáze: | Supplemental Index |
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