Ontogeny of the facial phenotypic variability in Mexican patients with 22q11.2 deletion syndrome

BACKGROUND: 22q11.2 deletion syndrome is a medical condition that results from genomic loss at chromosome 22. Affected patients exhibit large variability that ranges from a severe condition to mild symptoms. In addition, the spectrum of clinical features differs among populations and even within fam...

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Detalles Bibliográficos
Autores principales: Farrera, Arodi, Villanueva, María, Vizcaíno, Alfredo, Medina-Bravo, Patricia, Balderrábano-Saucedo, Norma, Rives, Mariana, Cruz, David, Hernández-Carbajal, Elizabeth, Granados-Riveron, Javier, Sánchez-Urbina, Rocío
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6905036/
https://www.ncbi.nlm.nih.gov/pubmed/31829202
http://dx.doi.org/10.1186/s13005-019-0213-9

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