Prenatal diagnosis of a de novo interstitial deletion of 11q (11q22.3 → q23.3) associated with abnormal ultrasound findings by array comparative genomic hybridization

BACKGROUND: Conventional G-band karyotyping offers low-resolution detection of chromosome abnormalities and cannot provide information about the involved genomic content. On the other hand, array comparative genomic hybridization can offer a rapid and comprehensive detection of genomewide gains and...

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Detalles Bibliográficos
Autores principales: Liu, Nian, Yan, Jiong, Chen, Xinlin, Song, Jieping, Wang, Bo, Yao, Yanyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189608/
https://www.ncbi.nlm.nih.gov/pubmed/25298785
http://dx.doi.org/10.1186/s13039-014-0062-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189608/
https://www.ncbi.nlm.nih.gov/pubmed/25298785
http://dx.doi.org/10.1186/s13039-014-0062-y

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