Aguinaga M - Search Results

1

Heterogeneous Diagnoses Underlying Radial Ray Anomalies.

Sevilla-Montoya R, Aguinaga M, Martínez A, Razo G, Molina B, Frías S, Grether P. Sevilla-Montoya R, et al. Among authors: aguinaga m. Indian J Pediatr. 2017 Mar;84(3):200-205. doi: 10.1007/s12098-016-2270-4. Epub 2016 Dec 17. Indian J Pediatr. 2017. PMID: 27987078

2

Prenatal diagnosis of trisomy 21 without the Down syndrome phenotype.

Aguinaga M, Razo G, Castro J, Mayén-Molina DG. Aguinaga M, et al. Prenat Diagn. 2006 Dec;26(12):1168-71. doi: 10.1002/pd.1583. Prenat Diagn. 2006. PMID: 17042031

3

The genetics of recurrent hydatidiform moles in Mexico: further evidence of a strong founder effect for one mutation in NLRP7 and its widespread.

Aguinaga M, Rezaei M, Monroy I, Mechtouf N, Pérez J, Moreno E, Valdespino Y, Galaz C, Razo G, Medina D, Piña R, Slim R. Aguinaga M, et al. J Assist Reprod Genet. 2021 Jul;38(7):1879-1886. doi: 10.1007/s10815-021-02132-1. Epub 2021 Mar 22. J Assist Reprod Genet. 2021. PMID: 33751332 Free PMC article.

4

Chromosome analysis of 303 pregnancy losses in Mexico.

Garduño-Zarazúa LM, Mayén DG, Meléndez-Hernández R, Paz-Martínez AJ, Ramírez-Arroyo E, Sosa D, Aguinaga M, Pérez-Durán J, Ríos O, López-Valdez J, Torres L, Frias S. Garduño-Zarazúa LM, et al. Among authors: aguinaga m. Gac Med Mex. 2024;160(1):76-85. doi: 10.24875/GMM.M24000859. Gac Med Mex. 2024. PMID: 38753554 English.

5

Causal analysis of fetal death in high-risk pregnancies.

Aguinaga M, Valdespino Y, Medina D, Espino Y Sosa S, Sevilla R, Miranda O, Acevedo S, Monroy IE, Helguera AC, Pérez J, Mariscal LF, Murillo MR, Lara RM, Armijos JC, Rogel G, Cardona JA. Aguinaga M, et al. J Perinat Med. 2021 Mar 19;49(6):740-747. doi: 10.1515/jpm-2020-0352. Print 2021 Jul 27. J Perinat Med. 2021. PMID: 33735952

6

The p.L750V mutation in the NLRP7 gene is frequent in Mexican patients with recurrent molar pregnancies and is not associated with recurrent pregnancy loss.

Estrada H, Buentello B, Zenteno JC, Fiszman R, Aguinaga M. Estrada H, et al. Among authors: aguinaga m. Prenat Diagn. 2013 Mar;33(3):205-8. doi: 10.1002/pd.4036. Epub 2013 Jan 28. Prenat Diagn. 2013. PMID: 23354651

7

Triphalangeal thumb and brachyectrodactyly syndrome: an uncommon entity with evidence of geographic distribution.

Zenteno JC, Aguinaga M, Chávez V, Sastré N, Rivera MR, Kofman-Alfaro S. Zenteno JC, et al. Among authors: aguinaga m. Clin Genet. 1996 Sep;50(3):152-5. doi: 10.1111/j.1399-0004.1996.tb02371.x. Clin Genet. 1996. PMID: 8946115

8

Sonic hedgehog mutation analysis in patients with VACTERL association.

Aguinaga M, Zenteno JC, Pérez-Cano H, Morán V. Aguinaga M, et al. Am J Med Genet A. 2010 Mar;152A(3):781-3. doi: 10.1002/ajmg.a.33293. Am J Med Genet A. 2010. PMID: 20186790 No abstract available.

9

Novel sonic hedgehog mutation in a couple with variable expression of holoprosencephaly.

Aguinaga M, Llano I, Zenteno JC, Kofman Alfaro S. Aguinaga M, et al. Case Rep Genet. 2011;2011:703497. doi: 10.1155/2011/703497. Epub 2011 Sep 8. Case Rep Genet. 2011. PMID: 23074678 Free PMC article.

10

Prenatal clinical characteristics of Casamassima-Morton-Nance syndrome.

Aguinaga M, Yllescas E, Canseco M, Machuca A, Acevedo S, Mayén Molina DG. Aguinaga M, et al. Prenat Diagn. 2009 Feb;29(2):175-6. doi: 10.1002/pd.2168. Prenat Diagn. 2009. PMID: 19090487 No abstract available.

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