Á lódáil...
Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype
Na minha lista:
| Foilsithe in: | Am J Kidney Dis |
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| Main Authors: | , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2017
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5890439/ https://ncbi.nlm.nih.gov/pubmed/28456345 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1053/j.ajkd.2017.03.017 |
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