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Transcriptomic Analysis of Cell-Free Fetal RNA Suggests a Specific Molecular Phenotype in Trisomy 18
BACKGROUND: Trisomy 18 is a common human aneuploidy that is associated with significant perinatal mortality. Unlike the well-characterized “critical region” in trisomy 21 (21q22), there is no corresponding region on chromosome 18 associated with its pathogenesis. The high morbidity and mortality of...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3206603/ https://ncbi.nlm.nih.gov/pubmed/21152935 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-010-0923-3 |
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