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Submicroscopic aberrations of chromosome 16 in prenatal diagnosis
BACKGROUND: Nearly 9.89% of chromosome 16 consists of segmental duplications, which makes it prone to non-homologous recombination. The present study aimed to investigate the incidence and perinatal characteristics of submicroscopic chromosome 16 aberrations in prenatal diagnosis. RESULTS: A total o...
Gorde:
| Argitaratua izan da: | Mol Cytogenet |
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| Egile Nagusiak: | , , , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BioMed Central
2019
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6681493/ https://ncbi.nlm.nih.gov/pubmed/31391865 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-019-0448-y |
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