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Did you mean alessandra stella (126 results)?
CYP21A2 intronic variants causing 21-hydroxylase deficiency.
Concolino P, Rizza R, Costella A, Carrozza C, Zuppi C, Capoluongo E. Concolino P, et al. Among authors: costella a. Metabolism. 2017 Jun;71:46-51. doi: 10.1016/j.metabol.2017.03.003. Epub 2017 Mar 9. Metabolism. 2017. PMID: 28521877 Review.
Multidisciplinary team for elucidation of any new mutation and how this approach can be useful to individualize any genetic result: the case of BRCA2 c.631G>A/c.7008-2A>T genotype Response to: Nagy PL, Mansukhani M. The role of clinical genomic testing in diagnosis and discovery of pathogenic mutations. Expert Rev Mol Diagn 2015;15(9):1101-5.
Minucci A, De Bonis M, Costella A, Scambia G, Scandurra G, Capoluongo E. Minucci A, et al. Among authors: costella a. Expert Rev Mol Diagn. 2016 Jul;16(7):715-7. doi: 10.1080/14737159.2016.1184573. Epub 2016 May 17. Expert Rev Mol Diagn. 2016. PMID: 27125725 No abstract available.
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