Congenital Heart Defects and Dysmorphic Facial Features in Patients Suspicious of 22q11.2 Deletion Syndrome in Southern Brazil

22q11.2 deletion syndrome (22q11.2DS) is considered one of the most frequently observed chromosomal abnormalities in association with congenital heart disease (CHD), which can also include some combination of other features. Thus, the aim of this work was to verify the profile of dysmorphic features...

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Detalhes bibliográficos
Publicado no:J Pediatr Genet
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Georg Thieme Verlag KG 2020
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7384886/
https://ncbi.nlm.nih.gov/pubmed/32733742
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0040-1713155
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