Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mariana Rives"'
Autor:
Arodi Farrera, María Villanueva, Alfredo Vizcaíno, Patricia Medina-Bravo, Norma Balderrábano-Saucedo, Mariana Rives, David Cruz, Elizabeth Hernández-Carbajal, Javier Granados-Riveron, Rocío Sánchez-Urbina
Publikováno v:
Head & Face Medicine, Vol 15, Iss 1, Pp 1-12 (2019)
Abstract 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 clini
Externí odkaz:
https://doaj.org/article/4befd271a73f4c04b2b2a8f0241efdfe
Autor:
David Cruz, Mariana Rives, María Villanueva, Norma Balderrabano-Saucedo, Arodi Farrera, Patricia G. Medina-Bravo, Elizabeth Hernández-Carbajal, Javier Granados-Riveron, Alfredo Vizcaíno, Rocío Sánchez-Urbina
Publikováno v:
Head & Face Medicine
Head & Face Medicine, Vol 15, Iss 1, Pp 1-12 (2019)
Head & Face Medicine, Vol 15, Iss 1, Pp 1-12 (2019)
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 featu