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A Pediatric Case of Dilated Cardiomyopathy Due to NKX2-5 Mutation : Autopsy and Postmortem Molecular Diagnosis.
Am J Forensic Med Pathol. 2024 Dec 1;45(4):e110-e112. doi: 10.1097/PAF.0000000000000967. Epub 2024 Jun 25.
Am J Forensic Med Pathol. 2024.
PMID: 39018455
No abstract available.
PRPH2-Related Retinal Dystrophies: Mutational Spectrum in 103 Families from a Spanish Cohort.
Fernández-Caballero L, Martín-Merida I, Blanco-Kelly F, Avila-Fernandez A, Carreño E, Fernandez-San Jose P, Irigoyen C, Jimenez-Rolando B, Lopez-Grondona F, Mahillo I, Martin-Gutierrez MP, Minguez P, Perea-Romero I, Del Pozo-Valero M, Riveiro-Alvarez R, Rodilla C, Rodriguez-Peña L, Sánchez-Barbero AI, Swafiri ST, Trujillo-Tiebas MJ, Zurita O, García-Sandoval B, Corton M, Ayuso C.
Fernández-Caballero L, et al. Among authors: sanchez barbero ai.
Int J Mol Sci. 2024 Mar 2;25(5):2913. doi: 10.3390/ijms25052913.
Int J Mol Sci. 2024.
PMID: 38474159
Free PMC article.
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Protein and genetic expression of CDKN1C and IGF2 and clinical features related to human umbilical cord length.
Olaya-C M, Ayala-Ramirez P, Sanchez-Barbero AI, Guzmán-P SL, Gil F, Silva JL; Seedbed in Perinatal Medicine; Bernal JE.
Olaya-C M, et al. Among authors: sanchez barbero ai.
J Perinat Med. 2020 May 1;49(2):229-236. doi: 10.1515/jpm-2019-0442. Print 2021 Feb 23.
J Perinat Med. 2020.
PMID: 32364515
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