Found: 8
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Recognizing genetic disease: A key aspect of pediatric pulmonary care.
- Published in:
- Pediatric Pulmonology, 2020, v. 55, n. 7, p. 1794, doi. 10.1002/ppul.24706
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- Publication type:
- Article
The future is here: Integrating genetics into the pediatric pulmonary clinic.
- Published in:
- Pediatric Pulmonology, 2020, v. 55, n. 7, p. 1810, doi. 10.1002/ppul.24723
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- Publication type:
- Article
Do mesenchymal stromal cell infusions advance the understanding and treatment options of FLNA‐associated pulmonary disease?
- Published in:
- Pediatric Pulmonology, 2020, v. 55, n. 2, p. 270, doi. 10.1002/ppul.24570
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- Publication type:
- Article
Association of Rare Pathogenic DNA Variants for Familial Hypercholesterolemia, Hereditary Breast and Ovarian Cancer Syndrome, and Lynch Syndrome With Disease Risk in Adults According to Family History.
- Published in:
- JAMA Network Open, 2020, v. 3, n. 4, p. e203959, doi. 10.1001/jamanetworkopen.2020.3959
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- Article
New insights into pulmonary hemorrhage.
- Published in:
- Pediatric Investigation, 2019, v. 3, n. 4, p. 207, doi. 10.1002/ped4.12170
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- Article
Personalized Cancer Monitoring Assay for the Detection of ctDNA in Patients with Solid Tumors.
- Published in:
- Molecular Diagnosis & Therapy, 2023, v. 27, n. 6, p. 753, doi. 10.1007/s40291-023-00670-1
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- Article
An assessment of the role of vinculin loss of function variants in inherited cardiomyopathy.
- Published in:
- Human Mutation, 2020, v. 41, n. 9, p. 1577, doi. 10.1002/humu.24061
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- Article
The expansive role of oxylipins on platelet biology.
- Published in:
- Journal of Molecular Medicine, 2017, v. 95, n. 6, p. 575, doi. 10.1007/s00109-017-1542-4
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- Article