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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Rare Diseases
Last data update: Apr 25, 2024
. (Total: 63675 Documents since 2012)
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Characterization of Autoimmune Thyroid Disease in a Cohort of 73 Paediatric Patients Affected by 22q11.2 Deletion Syndrome: Longitudinal Single-Centre Study.
Ricci Silvia et al. Genes 2022 13(9)
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Recurrence of Graves' Disease: What Genetics of HLA and PTPN22 Can Tell Us.
Vejrazkova Daniela et al. Frontiers in endocrinology 2021 12761077
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Aggregation of autoimmunity in extended families of people with autoimmune Addison's disease.
Fichna Marta et al. Internal medicine journal 2021
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A Weighted Genetic Risk Score Using Known Susceptibility Variants to Predict Graves Disease Risk.
Ma Yu-Ru et al. The Journal of clinical endocrinology and metabolism 2019 104(6) 2121-2130
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Progress in pediatrics in 2015: choices in allergy, endocrinology, gastroenterology, genetics, haematology, infectious diseases, neonatology, nephrology, neurology, nutrition, oncology and pulmonology.
Caffarelli Carlo et al. Italian journal of pediatrics 2016 Aug 42(1) 75
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Utility of systematic TSHR gene testing in adults with hyperthyroidism lacking overt autoimmunity and diffuse uptake on thyroid scintigraphy.
Patel Kashyap A et al. Clinical endocrinology 2018 Oct
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A MicroRNA Signature for Evaluation of Risk and Severity of Autoimmune Thyroid Diseases.
Martínez-Hernández Rebeca et al. The Journal of clinical endocrinology and metabolism 2018 103(3) 1139-1150
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 25, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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