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Importance of genetic study in primary hyperoxaluria type1. Case report.
Med Clin (Barc). 2024 Nov 3:S0025-7753(24)00566-9. doi: 10.1016/j.medcli.2024.07.027. Online ahead of print.
Med Clin (Barc). 2024.
PMID: 39489640
English, Spanish.
No abstract available.
Identification of hereditary breast and ovarian cancer germline variants in Granada (Spain): NGS perspective.
Molina-Zayas M, Garrido-Navas C, García-Puche JL, Barwell J, Pedrinaci S, Atienza MM, García-Linares S, de Haro-Muñoz T, Lorente JA, Serrano MJ, Poyatos-Andújar A.
Molina-Zayas M, et al.
Mol Genet Genomics. 2022 May;297(3):859-871. doi: 10.1007/s00438-022-01891-5. Epub 2022 Apr 22.
Mol Genet Genomics. 2022.
PMID: 35451682
Free PMC article.
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