Found: 12
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Implementation of high‐resolution melting analysis of the porcupine (PORCN) gene for molecular diagnosis of focal dermal hypoplasia: Identification of a novel mutation.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 5, p. 1, doi. 10.1002/jgm.3165
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- Article
Identification of human miR‐1839‐5p by small RNA‐seq, a miRNA enriched in neoplastic tissues.
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- Journal of Gene Medicine, 2019, v. 21, n. 10, p. N.PAG, doi. 10.1002/jgm.3117
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- Article
Daño al ADN en neonatos de madres con sobrepeso.
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- Revista Médica MD, 2017, v. 8, n. 4, p. 141
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- Article
Diet and Maternal Obesity Are Associated with Increased Oxidative Stress in Newborns: A Cross-Sectional Study.
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- Nutrients, 2022, v. 14, n. 4, p. 746, doi. 10.3390/nu14040746
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- Article
Genotyping of the Major SARS-CoV-2 Clade by Short-Amplicon High-Resolution Melting (SA-HRM) Analysis.
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- Genes, 2021, v. 12, n. 4, p. 531, doi. 10.3390/genes12040531
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- Article
Maternal obesity increases oxidative stress in the newborn.
- Published in:
- Obesity (19307381), 2015, v. 23, n. 8, p. 1650, doi. 10.1002/oby.21159
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- Article
Diabetes and obesity during pregnancy are associated with oxidative stress genotoxicity in newborns.
- Published in:
- Journal of Perinatal Medicine, 2019, v. 47, n. 3, p. 347, doi. 10.1515/jpm-2018-0201
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- Article
VHL mutation as a cause of three generations familial pheochromocytoma.
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- 2024
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- Publication type:
- Case Study
Genetic structure of three Native Mexican communities based on mtDNA haplogroups, and ABO and Rh blood group systems.
- Published in:
- Clinical & Translational Investigation / Revista de Investigación Clínica, 2011, v. 63, n. 6, p. 614
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- Article
Genetic polymorphisms associated with pediatric‐onset type 2 diabetes: A family‐based transmission disequilibrium test and case‐control study.
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- Pediatric Diabetes, 2019, v. 20, n. 3, p. 239, doi. 10.1111/pedi.12818
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- Article
Ontogeny of the facial phenotypic variability in Mexican patients with 22q11.2 deletion syndrome.
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- Head & Face Medicine, 2019, v. 15, n. 1, p. 1, doi. 10.1186/s13005-019-0213-9
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- Article
Opitz GBBB syndrome with total anomalous pulmonary venous connection: A new MID1 gene variant.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 9, p. 1, doi. 10.1002/mgg3.2234
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- Article