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1 . Academic Journal
Omics-based biomarkers: current status and potential use in the clinic
저자
by
Quezada, Héctor
;
Guzmán-Ortiz, Ana Laura
;
Díaz-Sánchez, Hugo
;
Valle-Rios, Ricardo
;
Aguirre-Hernández, Jesús
.
소스
In
Boletín Médico del Hospital Infantil de México
May-June 2017 74(3):219-226
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7 . Academic Journal
Fenotipo de miopatía congénita central core autosómica dominante con alteraciones del gen RYR1. A propósito de un caso clínico.
저자
by
Quintana-Vega, Verónica Joomayra
;
Barragán-Pérez, Eduardo Javier
;
Alarcón-De la Luz, Edwin Manolo
;
Alarcón-Cabrera, Ernesto
;
Sadowinski-Pine, Stanislaw
, et al.
소스
Acta Pediatrica de Mexico
. 2022, Vol. 43 Issue 6, p353-357. 5p.
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7 . Academic Journal
Classic infantile‐onset Pompe disease with histopathological neurologic findings linked to a novel GAA gene 4 bp deletion: A case study.
저자
by
Cerón‐Rodríguez, Magdalena
;
Castillo‐García, Daniela
;
Acosta‐Rodríguez‐Bueno, Carlos‐Patricio
;
Aguirre‐Hernández, Jesús
;
Murillo‐Eliosa, Juan‐Rafael
, et al.
소스
Molecular Genetics & Genomic Medicine
. Jul2022, Vol. 10 Issue 7, p1-9. 9p.
Open Access (Wiley)
Web of Science
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7 . Academic Journal
High penetrance of EDA pathogenic variants in Mexican female carriers with hypohidrotic ectodermal dysplasia.
저자
by
García-Delgado, Constanza
;
Noriega-Juárez, Miguel
;
Cervantes, Alicia
;
Abad-Flores, José
;
Toledo-Bahena, Mirna
, et al.
소스
Dermatologica Sinica; Jul-Sep2020, Vol. 38 Issue 3, p172-175, 4p
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7 . Academic Journal
Exploring single nucleotide polymorphisms previously related to obesity and metabolic traits in pediatric-onset type 2 diabetes.
저자
by
Miranda-Lora, América
;
Cruz, Miguel
;
Aguirre-Hernández, Jesús
;
Molina-Díaz, Mario
;
Gutiérrez, Jorge
, et al.
소스
Acta Diabetologica
. Jul2017, Vol. 54 Issue 7, p653-662. 10p.
Web of Science
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7 . Academic Journal
A novel nonsense LAMP2 variant associated with Danon disease in a pediatric male: A case report.
저자
by
Castillo-Garcia, Daniela
;
Cerón-Rodriguez, Magdalena
;
Acosta-Rodriguez-Bueno, Carlos Patricio
;
Aguirre-Hernández, Jesús
;
Almanza-Aranda, Judith
, et al.
소스
Molecular Genetics & Metabolism
. Feb2021, Vol. 132 Issue 2, pS23-S24. 2p.
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7 . Academic Journal
Importance of the diagnosis of protein connexin 26 mutations in the integral management of nonsyndromic congenital deafness.
저자
by
Mendelsberg-Fishbein, Paola
;
Márquez-Ávila, Candy Sue
;
García-Delgado, Constanza
;
Sánchez Boiso, Adriana
;
Rodríguez-Espino, Benjamín Antonio
, et al.
소스
Boletín Médico del Hospital Infantil de México
. mar/abr2013, Vol. 70 Issue 2, p88-96. 9p.
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7 . Academic Journal
Multiple Mechanisms Contribute to Leakiness of a Frameshift Mutation in Canine Cone-Rod Dystrophy.
저자
by
Miyadera, Keiko
;
Brierley, Ian
;
Aguirre-Hernández, Jesús
;
Mellersh, Cathryn S.
;
Sargan, David R.
.
소스
PLoS ONE
. Dec2012, Vol. 7 Issue 12, p1-10. 10p.
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7 . Academic Journal
DLA Class II Alleles and Haplotypes Are Associated with Risk for and Protection from Chronic Hepatitis in the English Springer Spaniel.
저자
by
Bexfield, Nicholas H.
;
Watson, Penny J.
;
Aguirre-Hernandez, Jesús
;
Sargan, David R.
;
Tiley, Laurence
, et al.
소스
PLoS ONE
. Aug2012, Vol. 7 Issue 8, Special section p1-7. 7p.
Web of Science
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7 . Academic Journal
Genetic structure of three Native Mexican communities based on mtDNA haplogroups, and ABO and Rh blood group systems.
저자
by
Sánchez-Boiso, Adriana
;
Peñaloza-Espinosa, Rosenda I.
;
Castro-Sierra, Eduardo
;
Cerda-Flores, Ricardo M.
;
Buentello-Malo, Leonora
, et al.
소스
Clinical & Translational Investigation / Revista de Investigación Clínica; nov/dec2011, Vol. 63 Issue 6, p614-620, 7p
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