Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencing

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Bibliografske podrobnosti
izdano v:Prenat Diagn
Main Authors: Macera, M.J., Sobrino, A., Levy, B., Jobanputra, V., Aggarwal, V., Mills, A., Esteves, C., Hanscom, C., Pereira, S., Pillalamarri, V., Ordulu, Z., Morton, C., Talkowski, M., Warburton, D.
Format: Artigo
Jezik:Inglês
Izdano: 2015
Teme:
Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4668937/
https://ncbi.nlm.nih.gov/pubmed/25043231
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pd.4456
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