Prenatal detection of unbalanced chromosomal rearrangements by array CGH

BACKGROUND: Karyotype analysis has been the standard method for prenatal cytogenetic diagnosis since the 1970s. Although highly reliable, the major limitation remains the requirement for cell culture, resulting in a delay of as much as 14 days to obtaining test results. Fluorescent in situ hybridisa...

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Hlavní autoři: Rickman, L, Fiegler, H, Shaw‐Smith, C, Nash, R, Cirigliano, V, Voglino, G, Ng, B L, Scott, C, Whittaker, J, Adinolfi, M, Carter, N P, Bobrow, M
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Group 2006
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2563226/
https://ncbi.nlm.nih.gov/pubmed/16199537
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2005.037648
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