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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)
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Last data update: Apr 18, 2024
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Hemophilia[original query]>>Guidelines Related[Product Type]
Novel F8 and F9 gene variants from the PedNet Hemophilia Registry classified according to ACMG/AMP guidelines.
Andersson Nadine G et al. Human mutation 2020 Sep
Similar articles in PubMed
Recommendations for the clinical interpretation of genetic variants and presentation of results to patients with inherited bleeding disorders. A UK Haemophilia Centre Doctors' Organisation Good Practice Paper.
Gomez Keith et al. Haemophilia : the official journal of the World Federation of Hemophilia 2019 Jan 25(1) 116-126
Similar articles in PubMed
Consensus Statement of the Indian Academy of Pediatrics in Diagnosis and Management of Hemophilia.
Sachdeva Anupam et al. Indian pediatrics 2018 Jul 55(7) 582-590
Similar articles in PubMed
Joint SOGC-CCMG Opinion for Reproductive Genetic Carrier Screening: An Update for All Canadian Providers of Maternity and Reproductive Healthcare in the Era of Direct-to-Consumer Testing.
Wilson R Douglas et al. Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obste´trique et gyne´cologie du Canada : JOGC 2016 Aug 38(8) 742-762.e3
Similar articles in PubMed
MASAC Recommendations on Standardized Testing and Surveillance for Inhibitors in Patients with Hemophilia A and B,
National Hemophilia Foundation, October 6, 2015
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 18, 2024
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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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