Last Posted: Jan 31, 2019
- Diagnostic yield and clinical utility of a comprehensive gene panel for hereditary tumor syndromes.
Henn Jonas et al. Hereditary cancer in clinical practice 2019 175 - 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 - Genomic medicine and incidental findings: balancing actionability and patient autonomy.
McCormick Jennifer B et al. Mayo Clinic proceedings 2014 Jun 89(6) 718-21 - Identification of Misclassified ClinVar Variants via Disease Population Prevalence.
Shah Naisha et al. American journal of human genetics 2018 102(4) 609-619 - Return of individual genomic research results: are laws and policies keeping step?
Thorogood Adrian et al. European journal of human genetics : EJHG 2019 Jan - Role and practice evolution for genetic counseling in the genomic era: The experience of Australian and UK genetics practitioners.
Dwarte Tanya et al. Journal of genetic counseling 2018 Dec - Ethical conundrums in pediatric genomics.
Rotz Seth J et al. Hematology. American Society of Hematology. Education Program 2018 Nov 2018(1) 301-306 - The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome Sequencing.
Rasouly Hila Milo et al. Annals of internal medicine 2018 Nov - [Performance of interpreting the variants of long QT syndrome according ACMG guidelines by four clinical gene screening agencies from Beijing].
Liu N et al. Zhonghua xin xue guan bing za zhi 2018 Nov 46(11) 857-861 - Wilson's Disease: A Review for the General Pediatrician.
Capone Kristin et al. Pediatric annals 2018 Nov 47(11) e440-e444
.png)
No hay comentarios:
Publicar un comentario