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2023 | 1 |
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Expanding the phenotype of PIGP deficiency to multiple congenital anomalies-hypotonia-seizures syndrome.
Clin Genet. 2023 Aug;104(2):245-250. doi: 10.1111/cge.14340. Epub 2023 May 1.
Clin Genet. 2023.
PMID: 37125481
Late-onset Familial Amyloidotic Polyneuropathy with Bence Jones Proteinuria and Cardiomyopathy.
García de León SC, González AH, Alonso CO, Lobo LB.
García de León SC, et al. Among authors: alonso co.
J Neurosci Rural Pract. 2017 Jul-Sep;8(3):448-450. doi: 10.4103/jnrp.jnrp_498_16.
J Neurosci Rural Pract. 2017.
PMID: 28694632
Free PMC article.
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Prenatal Genome-Wide Cell-Free DNA Screening: Three Years of Clinical Experience in a Hospital Prenatal Diagnostic Unit in Spain.
Pedrola Vidal L, Roselló Piera M, Martín-Grau C, Rubio Moll JS, Gómez Portero R, Marcos Puig B, Cervera Zamora JV, Quiroga R, Orellana Alonso C.
Pedrola Vidal L, et al. Among authors: orellana alonso c.
Genes (Basel). 2024 Apr 28;15(5):568. doi: 10.3390/genes15050568.
Genes (Basel). 2024.
PMID: 38790198
Free PMC article.
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