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Prenatal Genome-Wide Cell-Free DNA Screening: Three Years of Clinical Experience in a Hospital Prenatal Diagnostic Unit in Spain.
Genes (Basel). 2024 Apr 28;15(5):568. doi: 10.3390/genes15050568.
Genes (Basel). 2024.
PMID: 38790198
Free PMC article.
Expanding the phenotype of PIGP deficiency to multiple congenital anomalies-hypotonia-seizures syndrome.
Martín-Grau C, Orellana Alonso C, Roselló Piera M, Pedrola Vidal L, Llorens-Salvador R, Quiroga R, Marín Reina P, Rubio Moll JS, Gómez Portero R, Martínez-Castellano F.
Martín-Grau C, et al. Among authors: orellana alonso c.
Clin Genet. 2023 Aug;104(2):245-250. doi: 10.1111/cge.14340. Epub 2023 May 1.
Clin Genet. 2023.
PMID: 37125481
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Renal adenocarcinoma in an 8-year-old child, with a t(X;17)(p11.2;q25).
Hernandez-Martí MJ, Orellana-Alonso C, Badía-Garrabou L, Verdeguer Miralles A, Paradís-Alós A.
Hernandez-Martí MJ, et al. Among authors: orellana alonso c.
Cancer Genet Cytogenet. 1995 Aug;83(1):82-3. doi: 10.1016/0165-4608(94)00184-7.
Cancer Genet Cytogenet. 1995.
PMID: 7656211
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