Microarray testing in clinical diagnosis: an analysis of 5,300 New Zealand patients

BACKGROUND: The use of Microarray (array CGH) analysis has become a widely accepted front-line test replacing G banded chromosome studies for patients with an unexplained phenotype. We detail our findings of over 5300 cases. RESULTS: Of 5369 pre and postnatal samples, copy number variants (CNVs) wer...

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Detalles Bibliográficos
Autores principales: Mc Cormack, Adrian, Claxton, Karen, Ashton, Fern, Asquith, Philip, Atack, Edward, Mazzaschi, Roberto, Moverley, Paula, O’Connor, Rachel, Qorri, Methat, Sheath, Karen, Love, Donald R., George, Alice M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4815202/
https://www.ncbi.nlm.nih.gov/pubmed/27034718
http://dx.doi.org/10.1186/s13039-016-0237-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4815202/
https://www.ncbi.nlm.nih.gov/pubmed/27034718
http://dx.doi.org/10.1186/s13039-016-0237-9

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