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1.
Three Types of Immunodeficiency, Centromeric Instability, and Facial Anomalies (ICF) Syndrome Identified by Whole-Exome Sequencing in Saudi Hypogammaglobulinemia Patients: Clinical, Molecular, and Cytogenetic Features.
J Clin Immunol
; 38(8): 847-853, 2018 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-30511102
2.
Clinical Presentation and Management of Multisystem Inflammatory Syndrome in Children With COVID-19: A Systematic Review.
Cureus
; 15(10): e46918, 2023 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-37954764
3.
Multiple Family Members With Delayed Cord Separtion and Combined Immunodeficiency With Novel Mutation in IKBKB.
Front Pediatr
; 8: 9, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32117824
4.
Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies.
Genome Med
; 11(1): 38, 2019 06 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-31203817
5.
Biallelic RIPK1 mutations in humans cause severe immunodeficiency, arthritis, and intestinal inflammation.
Science
; 361(6404): 810-813, 2018 08 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-30026316
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