Cargando…
Prenatal Diagnosis of a Fetus with de novo Supernumerary Ring Chromosome 16 Characterized by Array Comparative Genomic Hybridization
A fetus with de novo ring chromosome 16 is presented. At 20 weeks' gestation, ultrasound examination demonstrated bilateral clubfoot, bilateral renal pyelectasis, hypoplasia of the corpus callosum, and transposition of the great vessel. Amniocentesis was performed. Chromosome analysis identifie...
Autores principales: | Cignini, Pietro, Dinatale, Angela, D'Emidio, Laura, Giacobbe, Annamaria, Pappalardo, Elisa Maria, Ermito, Santina, Bizzoco, Domenico, Di Giacomo, Gianluca, Gabrielli, Ivan, Mesoraca, Alvaro, Giorlandino, Maurizio, Giorlandino, Claudio |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Thieme Medical Publishers
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3653546/ https://www.ncbi.nlm.nih.gov/pubmed/23705081 http://dx.doi.org/10.1055/s-0031-1274512 |
Ejemplares similares
-
Next Generation Sequencing Approach in a Prenatal Case of Cardio-Facio-Cutaneus Syndrome
por: Mucciolo, Mafalda, et al.
Publicado: (2016) -
Ultrasonographic evaluation of placental cord insertion at different gestational ages in low-risk singleton pregnancies: a predictive algorithm
por: Padula, F, et al.
Publicado: (2016) -
Reference Charts for Fetal Cerebellar Vermis Height: A Prospective Cross-Sectional Study of 10605 Fetuses
por: Cignini, Pietro, et al.
Publicado: (2016) -
De novo 3q13.13q21.2 interstitial deletion and paternal 12p13.3 microdeletion in a fetus with dysplasia of the corpus callosum and ventriculomegaly: A case report
por: Libotte, Francesco, et al.
Publicado: (2023) -
Prenatal Diagnosis of Combined Maternal 4q Interstitial Deletion and Paternal 15q Microduplication
por: Libotte, Francesco, et al.
Publicado: (2021)