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Gene Variants in NKX2-1 Do Not Represent a Major Etiological Factor of Primary Congenital Hypothyroidism in Mexican Population.
J Pediatr Genet. 2019 Jun;8(2):41-46. doi: 10.1055/s-0038-1676644. Epub 2019 Jan 2.
J Pediatr Genet. 2019.
PMID: 31061744
Free PMC article.
Germline mutations in NKX2-5, GATA4, and CRELD1 are rare in a Mexican sample of Down syndrome patients with endocardial cushion and septal heart defects.
Alcántara-Ortigoza MA, De Rubens-Figueroa J, Reyna-Fabian ME, Estandía-Ortega B, González-del Angel A, Molina-Álvarez B, Velázquez-Aragón JA, Villagómez-Martínez S, Pereira-López GI, Martínez-Cruz V, Álvarez-Gómez RM, Díaz-García L.
Alcántara-Ortigoza MA, et al. Among authors: martinez cruz v.
Pediatr Cardiol. 2015 Apr;36(4):802-8. doi: 10.1007/s00246-014-1091-3. Epub 2014 Dec 19.
Pediatr Cardiol. 2015.
PMID: 25524324
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Erratum to: Germline Mutations in NKX2-5, GATA4, and CRELD1 are Rare in a Mexican Sample of Down Syndrome Patients with Endocardial Cushion and Septal Heart Defects.
Alcántara-Ortigoza MA, De Rubens-Figueroa J, Reyna-Fabian ME, Estandía-Ortega B, González-Del Angel A, Molina-Álvarez B, Velázquez-Aragón JA, Villagómez-Martínez S, Pereira-López GI, Martínez-Cruz V, Álvarez-Gómez RM, Díaz-García L.
Alcántara-Ortigoza MA, et al. Among authors: martinez cruz v.
Pediatr Cardiol. 2015 Oct;36(7):1551. doi: 10.1007/s00246-015-1226-1.
Pediatr Cardiol. 2015.
PMID: 26205256
No abstract available.
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Expansion of the variable expression of Muenke syndrome: Hydrocephalus without craniosynostosis.
González-Del Angel A, Estandía-Ortega B, Alcántara-Ortigoza MA, Martínez-Cruz V, Gutiérrez-Tinajero DJ, Rasmussen A, Gómez-González CS.
González-Del Angel A, et al. Among authors: martinez cruz v.
Am J Med Genet A. 2016 Dec;170(12):3189-3196. doi: 10.1002/ajmg.a.37951. Epub 2016 Aug 29.
Am J Med Genet A. 2016.
PMID: 27568649
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Low allelic heterogeneity in a sample of Mexican patients with classical galactosaemia.
Velázquez-Aragón J, Alcántara-Ortigoza MA, Vela-Amieva M, Monroy S, Martínez-Cruz V, Todd-Quiñones C, González-del Angel A.
Velázquez-Aragón J, et al. Among authors: martinez cruz v.
J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S333-7. doi: 10.1007/s10545-008-0905-y. Epub 2008 Oct 29.
J Inherit Metab Dis. 2008.
PMID: 18956253
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Molecular analysis of the PAX8 gene in a sample of Mexican patients with primary congenital hypothyroidism: identification of the recurrent p.Arg31His mutation.
Alcántara-Ortigoza MA, González-del Angel A, Martínez-Cruz V, Vela-Amieva M, Sánchez-Pérez C, Moreno-Rojas R, Estandía-Ortega B, Hernández-Martínez N.
Alcántara-Ortigoza MA, et al. Among authors: martinez cruz v.
Clin Endocrinol (Oxf). 2012 Jan;76(1):148-50. doi: 10.1111/j.1365-2265.2011.04153.x.
Clin Endocrinol (Oxf). 2012.
PMID: 21689132
No abstract available.
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Histone deacetylases modulate resistance to the therapy in lung cancer.
Contreras-Sanzón E, Prado-Garcia H, Romero-Garcia S, Nuñez-Corona D, Ortiz-Quintero B, Luna-Rivero C, Martínez-Cruz V, Carlos-Reyes Á.
Contreras-Sanzón E, et al. Among authors: martinez cruz v.
Front Genet. 2022 Oct 3;13:960263. doi: 10.3389/fgene.2022.960263. eCollection 2022.
Front Genet. 2022.
PMID: 36263432
Free PMC article.
Review.
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