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Copy number variations associated with fetal congenital kidney malformations
BACKGROUND: Congenital anomalies of the kidney and urinary tract (CAKUT) constitute 20–30% of all congenital malformations. Within the CAKUT phenotypic spectrum, renal hypodysplasia (RHD) is particularly severe. This study aimed to evaluate the applicability of single-nucleotide polymorphism (SNP) a...
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| Опубликовано в: : | Mol Cytogenet |
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| Главные авторы: | , , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BioMed Central
2020
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7092440/ https://ncbi.nlm.nih.gov/pubmed/32211073 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-020-00481-7 |
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