Found: 13
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Polymorphisms of the gene encoding Kit ligand are associated with bronchopulmonary dysplasia.
- Published in:
- Pediatric Pulmonology, 2015, v. 50, n. 3, p. 260, doi. 10.1002/ppul.23018
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- Publication type:
- Article
Human placental proteomics and exon variant studies link AAT/SERPINA1 with spontaneous preterm birth.
- Published in:
- BMC Medicine, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12916-022-02339-8
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- Publication type:
- Article
A Potential Novel Spontaneous Preterm Birth Gene, AR, Identified by Linkage and Association Analysis of X Chromosomal Markers.
- Published in:
- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0051378
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- Article
Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2.
- Published in:
- PLoS Genetics, 2019, v. 15, n. 6, p. 1, doi. 10.1371/journal.pgen.1008107
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- Publication type:
- Article
Integrative genetic, genomic and transcriptomic analysis of heat shock protein and nuclear hormone receptor gene associations with spontaneous preterm birth.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-96374-9
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- Publication type:
- Article
Cerebral Palsy and Polymorphism of the Chemokine CCL18 in Very Preterm Children.
- Published in:
- Neonatology (16617800), 2015, v. 108, n. 2, p. 124, doi. 10.1159/000430765
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- Publication type:
- Article
Genes Encoding Vascular Endothelial Growth Factor A (VEGF-A) and VEGF Receptor 2 (VEGFR-2) and Risk for Bronchopulmonary Dysplasia.
- Published in:
- Neonatology (16617800), 2015, v. 108, n. 1, p. 53, doi. 10.1159/000381279
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- Publication type:
- Article
A study of genes encoding cytokines (IL6, IL10, TNF), cytokine receptors (IL6R, IL6ST), and glucocorticoid receptor (NR3C1) and susceptibility to bronchopulmonary dysplasia
- Published in:
- BMC Medical Genetics, 2014, v. 15, n. 1, p. 120, doi. 10.1186/s12881-014-0120-7
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- Publication type:
- Article
Human placental proteomics and exon variant studies link AAT/SERPINA1 with spontaneous preterm birth.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.
- Published in:
- 2018
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- Correction Notice
Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 7, p. 1, doi. 10.1371/journal.pgen.1007394
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- Publication type:
- Article
Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia.
- Published in:
- 2022
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- Publication type:
- corrected article
Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia.
- Published in:
- 2021
- By:
- Publication type:
- journal article