22q11.2 Deletion Syndrome due to a Translocation t(6;22) in a Patient Conceived via in vitro Fertilization.

Autor: Gollo Dantas A; Genetics Division, Department of Morphology and Genetics, Universidade Federal de São Paulo, Brazil., Bortolai A; Genetics Division, Department of Morphology and Genetics, Universidade Federal de São Paulo, Brazil; Cytogenetics Division, Hospital do Servidor Público do Estado de São Paulo, São Paulo, Brazil., Moysés-Oliveira M; Genetics Division, Department of Morphology and Genetics, Universidade Federal de São Paulo, Brazil., Takeno Herrero S; Genetics Division, Department of Morphology and Genetics, Universidade Federal de São Paulo, Brazil., Azoubel Antunes A; Hospital das Clínicas, Universidade Federal de Pernambuco, Recife, Brazil., Tavares Costa-Carvalho B; Division of Allergy, Clinical Immunology and Rheumatology, Universidade Federal de São Paulo, Brazil., Ayres Meloni V; Genetics Division, Department of Morphology and Genetics, Universidade Federal de São Paulo, Brazil., Melaragno MI; Genetics Division, Department of Morphology and Genetics, Universidade Federal de São Paulo, Brazil.

Publikováno v: Molecular syndromology [Mol Syndromol] 2016 Feb; Vol. 6 (5), pp. 242-7. Date of Electronic Publication: 2015 Nov 14.