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Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities
BACKGROUND: We have investigated whether replacing conventional karyotyping by SNP array analysis in cases of foetal ultrasound abnormalities would increase the diagnostic yield and speed of prenatal diagnosis in clinical practice. FINDINGS/RESULTS: From May 2009 till June 2011 we performed HumanCyt...
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| Autori principali: | , , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2012
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3328283/ https://ncbi.nlm.nih.gov/pubmed/22413963 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8166-5-14 |
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