Cargando…
Prenatal diagnosis and molecular cytogenetic characterization of a de novo duplication of 15q24.3-q26.1
Reported cases of distal 15q interstitial duplications are uncommon and do not result in a recognizable pattern of abnormalities. Some studies report prenatal overgrowth, while others describe growth retardation. We present molecular cytogenetic characterization of a 14 Mb interstitial duplication,...
Autores principales: | Ochando, Isabel, Martínez, Melanie Cristine Alonzo, Serrano, Ana María, Urbano, Antonio, Cazorla, Eduardo, Calvo, Dolores, Rueda, Joaquín |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6037148/ https://www.ncbi.nlm.nih.gov/pubmed/30013380 http://dx.doi.org/10.2147/TACG.S159377 |
Ejemplares similares
-
A case of de novo duplication of 15q24-q26.3
por: Kim, Eun Young, et al.
Publicado: (2011) -
Clinical and molecular characterization of a patient with a combination of a deletion and a duplication of 22q13 using array CGH
por: Ochando, Isabel, et al.
Publicado: (2012) -
A rare de novo duplication of chromosome 21q22.12 → q22.3 with other concomitant deletion and duplication of small fragments in 21q associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization
por: Qi, Qingwei, et al.
Publicado: (2013) -
Patient With Delayed Development Resulting From De Novo Duplication of 7q36.1-q36.3 and Deletion of 9p24.3
por: Choi, Asayeon, et al.
Publicado: (2017) -
Deletion polymorphism at chromosome 3q26.1 and oral squamous cell carcinoma
por: KAWACHI, HOMARE, et al.
Publicado: (2012)