المؤلفون: Dora Janeth Fonseca, Clara Esteban-Pérez, Sandrine Barbaux, María Alejandra Coronel, Elkin Lucena, Diego A. Ojeda, Diana Carolina Sierra-Diaz, Karen Marcela Jiménez, Paul Laissue, Sandra Bello, Daniel Vaiman, Paula Quintero-Ronderos, Harold Moreno-Ortiz

المصدر: Molecular Medicine, Vol 25, Iss 1, Pp 1-8 (2019)
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario
Molecular Medicine

مصطلحات موضوعية: 0301 basic medicine, Pregnancy disorder, Plgf gene, Pathogenesis, Repeated implantation failure, Gene sequence, Gene mutation, Bioinformatics, Gene, Plasmid, Cohort Studies, 0302 clinical medicine, Pre-Eclampsia, Pregnancy, Placental growth factor, In vitro fertilization, lcsh:QD415-436, Promoter Regions, Genetic, Genetics (clinical), Priority journal, Reimplantation, Fetal Growth Retardation, Genetic transcription, Sequence analysis, Forkhead Transcription Factors, Phenotype, Colombian, 030220 oncology & carcinogenesis, Molecular Medicine, Female, Human, Adult, Infertility, Abortion, Habitual, Genotype, Complement component C3, Short Report, Major clinical study, Biology, Polymorphism, Single Nucleotide, Article, Preeclampsia, lcsh:Biochemistry, 03 medical and health sciences, Genetic screening, Genetics, medicine, Humans, Genetic Predisposition to Disease, Molecular Biology, Fetus, Genetic regulation, Gene deletion, lcsh:RM1-950, In vitro study, Frenchman, FOXD1 gene, Intrauterine growth retardation, medicine.disease, C3 gene, 030104 developmental biology, lcsh:Therapeutics. Pharmacology, Gene identification, Mutation, Genetic variability, Controlled study

وصف الملف: text; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3e6cb15e50b18b0da7ec32c3cfaf10b
http://link.springer.com/article/10.1186/s10020-019-0104-3