Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Precision Health Database


Genomics & Health Impact Scan Database|Search|PHGKB

Rare Diseases

Last data update: Mar 27, 2023. (Total: 58931 Documents since 2012)
   dataset      
Filtered By:

Previous    

Records 1 - 5 (of 5 Records)

Query Trace: 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
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
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
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
MASAC Recommendations on Standardized Testing and Surveillance for Inhibitors in Patients with Hemophilia A and B,
National Hemophilia Foundation, October 6, 2015
TOP