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Page 1
Deep Phenotyping and Genetic Characterization of a Cohort of 70 Individuals With 5p Minus Syndrome.
Nevado J, Bel-Fenellós C, Sandoval-Talamantes AK, Hernández A, Biencinto-López C, Martínez-Fernández ML, Barrúz P, Santos-Simarro F, Mori-Álvarez MÁ, Mansilla E, García-Santiago FA, Valcorba I, Sáenz-Rico B, Martínez-Frías ML, Lapunzina P. Nevado J, et al. Among authors: sandoval talamantes ak. Front Genet. 2021 Jul 30;12:645595. doi: 10.3389/fgene.2021.645595. eCollection 2021. Front Genet. 2021. PMID: 34394178 Free PMC article.
Third case of Duchenne muscular dystrophy and West syndrome: Expanding the spectrum of the DMD neuropsychiatric phenotype.
Peña-Padilla C, Romero-Valenzuela I, Baldomero-López A, Sandoval-Talamantes AK, Castellanos-González A, Nagy PL, Kelly RR, Corona-Rivera JR. Peña-Padilla C, et al. Among authors: sandoval talamantes ak. Neuromuscul Disord. 2021 May;31(5):462-465. doi: 10.1016/j.nmd.2021.02.004. Epub 2021 Feb 9. Neuromuscul Disord. 2021. PMID: 33741226
GATA2 null mutation associated with incomplete penetrance in a family with Emberger syndrome.
Brambila-Tapia AJL, García-Ortiz JE, Brouillard P, Nguyen HL, Vikkula M, Ríos-González BE, Sandoval-Muñiz RJ, Sandoval-Talamantes AK, Bobadilla-Morales L, Corona-Rivera JR, Arnaud-Lopez L. Brambila-Tapia AJL, et al. Among authors: sandoval talamantes ak. Hematology. 2017 Sep;22(8):467-471. doi: 10.1080/10245332.2017.1294551. Epub 2017 Mar 8. Hematology. 2017. PMID: 28271814