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LUIS EDUARDO BECERRA SOLANO
LUIS EDUARDO BECERRA SOLANO
在 cualtos.udg.mx 的电子邮件经过验证
标题
引用次数
引用次数
年份
PEDIA: prioritization of exome data by image analysis
TC Hsieh, MA Mensah, JT Pantel, D Aguilar, O Bar, A Bayat, ...
Genetics in Medicine 21 (12), 2807-2814, 2019
942019
A missense mutation, p. V132G, in the X‐linked spermine synthase gene (SMS) causes Snyder–Robinson syndrome
LE Becerra‐Solano, J Butler, G Castaneda‐Cisneros, DE McCloskey, ...
American Journal of Medical Genetics Part A 149 (3), 328-335, 2009
732009
An update on amniotic bands sequence
E López-Muñoz, LE Becerra-Solano
Arch Argent Pediatr 116 (3), e409-e420, 2018
212018
Microcephaly, an etiopathogenic vision
LE Becerra-Solano, L Mateos-Sánchez, E López-Muñoz
Pediatrics & Neonatology 62 (4), 354-360, 2021
202021
Uncommon runs of homozygosity disclose homozygous missense mutations in two ciliopathy-related genes (SPAG17 and WDR35) in a patient with multiple brain and skeletal anomalies
C Córdova-Fletes, LE Becerra-Solano, MM Rangel-Sosa, ...
European Journal of Medical Genetics 61 (3), 161-167, 2018
202018
The fifth female patient with Myhre syndrome: further delineation
LE Becerra-Solano, M Díaz-Rodriguez, JA Nastasi-Catanese, ...
Clinical Dysmorphology 17 (2), 113-117, 2008
202008
Fisiopatología. La ciencia del porqué y el cómo
RAU Olivares
Elsevier Health Sciences, 2018
162018
Bosma arrhinia microphthalmia syndrome in a Mexican patient with a molecular analysis of PAX6
LE Becerra-Solano, L Chacón, D Morales-Mata, JC Zenteno, ...
Clinical Dysmorphology 25 (1), 12-15, 2016
132016
First case reported of Turner syndrome and trisomy 14 chromosomal mosaicism in a patient
LE Becerra-Solano, L Arnaud-Lopez, M Diaz-Rodriguez, ...
Clinical Dysmorphology 17 (1), 27-30, 2008
102008
Study of the interaction of Ti–Zn as a mixed oxide at different pH values synthesized by the sol–gel method and its antibacterial properties
N Rodríguez-Barajas, L Becerra-Solano, YK Gutiérrez-Mercado, ...
Nanomaterials 12 (12), 1948, 2022
92022
A study of Zn-Ca nanocomposites and their antibacterial properties
MI Torres-Ramos, UJ Martín-Camacho, JL González, MF Yañez-Acosta, ...
International Journal of Molecular Sciences 23 (13), 7258, 2022
62022
Secuencia de bandas amnióticas, una actualización
E López-Muñoz, LE Becerra-Solano
Archivos argentinos de pediatría 116 (3), e409-e420, 2018
62018
Severe craniofacial involvement due to amniotic band sequence
LE Becerra-Solano, G Castañeda-Cisneros, JR Corona-Rivera, ...
Fetal and Pediatric Pathology 37 (1), 27-37, 2018
52018
Whole-exome sequencing in three children with sporadic Blau syndrome, one of them co-presenting with recurrent polyserositis
C Córdova-Fletes, MM Rangel-Sosa, LA Martínez-Jacobo, ...
Autoimmunity 53 (6), 344-352, 2020
42020
Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder
JE García-Ortiz, AI Zarazúa-Niño, AA Hernández-Orozco, EA Reyes-Oliva, ...
Journal of Autism and Developmental Disorders 50, 2247-2251, 2020
42020
Benign familial macrocephaly in a mother-son pair
M Díaz-Rodríguez, LE Becerra-Solano, JJ Toscano-Flores, ...
Genetic Counseling 21 (1), 85, 2010
42010
Schilbach-Rott syndrome in a third family: further delineation of an autosomal dominant trait
LE Becerra-Solano, MP Casillas-Avila, M Dias-Rodriguez, ...
Genetic Counseling 18 (3), 317-324, 2007
42007
Hermafroditismo verdadero y secuencias del cromosoma Y. Implicaciones a propósito de dos casos
J de Jesús Toscano-Flores, J Padilla-Gutiérrez, L Becerra-Solano, ...
Revista Médica del Instituto Mexicano del Seguro Social 46 (5), 539-542, 2008
32008
Effects of SPTA1 Gene Variants on the Hematological Phenotype of Mexican Patients with Hereditary Spherocytosis
IM Herrera-Tirado, LL Espinoza-Mata, LC Rizo-delaTorre, ...
Genetic Testing and Molecular Biomarkers 26 (5), 270-276, 2022
22022
Causas del hidrops fetal: experiencia en un hospital obstétrico del Occidente de México
LE Becerra-Solano, M Medina-Castellanos, LF Oseguera-Torres, ...
Ginecología y obstetricia de México 90 (7), 579-589, 2022
12022
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