Cargando…
Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years’ clinical application for over 8,700 patients
BACKGROUND: Array CGH is widely used in cytogenetics centres for postnatal constitutional genome analysis, and is now recommended as a first line test in place of G-banded chromosome analysis. At our centre, first line testing by oligonucleotide array CGH for all constitutional referrals for genome...
Autores principales: | Ahn, Joo Wook, Bint, Susan, Bergbaum, Anne, Mann, Kathy, Hall, Richard P, Ogilvie, Caroline Mackie |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3632487/ https://www.ncbi.nlm.nih.gov/pubmed/23560982 http://dx.doi.org/10.1186/1755-8166-6-16 |
Ejemplares similares
-
Multicolor banding remains an important adjunct to array CGH and conventional karyotyping
por: Bint, Susan M, et al.
Publicado: (2013) -
Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance
por: Ahn, Joo Wook, et al.
Publicado: (2010) -
MLPA for confirmation of array CGH results and determination of inheritance
por: Hills, Alison, et al.
Publicado: (2010) -
Efficient and cost-effective genetic analysis of products of conception and fetal tissues using a QF-PCR/array CGH strategy; five years of data
por: Donaghue, Celia, et al.
Publicado: (2017) -
Whole-Genome Array CGH Evaluation for Replacing Prenatal Karyotyping in Hong Kong
por: Kan, Anita S. Y., et al.
Publicado: (2014)