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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
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Records 1 - 13 (of 13 Records)
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Li-fraumeni Syndrome[original query]>>Guidelines Related[Product Type]
NCCN Guidelines® Insights: Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 2.2024.
Mary B Daly et al. J Natl Compr Canc Netw 2023 21(10) 1000-1010
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Overview of the Clinical Features of Li-Fraumeni Syndrome and the Current European ERN GENTURIS Guideline.
Kratz Christian Peter et al. Geburtshilfe und Frauenheilkunde 2022 82(1) 42-49
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Medical guidelines for Li-Fraumeni syndrome 2019, version 1.1.
Kumamoto Tadashi et al. International journal of clinical oncology 2021
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Evaluation and comparison of hereditary Cancer guidelines in the population.
Ritchie Jordon B et al. Hereditary cancer in clinical practice 2021 19(1) 31
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Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants.
Fortuno Cristina et al. Human mutation 2020 Dec
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Guidelines for the Li–Fraumeni and heritable TP53-related cancer syndromes
T Frebourg et al, EJHG et al, May 26, 2020
Hereditary Cancer Syndromes and Risk Assessment: ACOG COMMITTEE OPINION SUMMARY, Number 793.
et al. Obstetrics and gynecology 2019 Dec 134(6) 1366-1367
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Local Coverage Determination (LCD): BRCA1 and BRCA2 Genetic Testing (L36715)
The U.S. Centers for Medicare & Medicaid Services
Local Coverage Determination (LCD): BRCA1 and BRCA2 Genetic Testing (L36499)
The U.S. Centers for Medicare & Medicaid Services
Recommendations for Surveillance for Children with Leukemia-Predisposing Conditions.
Porter Christopher C et al. Clinical cancer research : an official journal of the American Association for Cancer Research 2017 Jun 23(11) e14-e22
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Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome.
Kratz Christian P et al. Clinical cancer research : an official journal of the American Association for Cancer Research 2017 23(11) e38-e45
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Recommended Guidelines for Validation, Quality Control, and Reporting of TP53 Variants in Clinical Practice.
Leroy Bernard et al. Cancer research 2017 Mar
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Committee opinion no. 634: hereditary cancer syndromes and risk assessment.
Obstet Gynecol 2015 Jun 125(6) 1538-43
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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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