Last Posted: Aug 07, 2019
- Familial Cancer: How to Successfully Recruit Families for Germline Mutations Studies? Multiple Myeloma as an Example.
Blocka Joanna et al. Clinical lymphoma, myeloma & leukemia 2019 Jul - Pitfalls in interpretation of CFTR variants in the context of incidental findings.
Boussaroque Agathe et al. Human mutation 2019 Jul - Diagnostic yield of next-generation sequencing applied to neurological disorders.
Marques Matos Cláudia et al. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2019 Jul - Secondary findings from next generation sequencing: Psychological and ethical issues. Family and patient perspectives.
Houdayer F et al. European journal of medical genetics 2019 Jun 103711 - Preimplantation genetic testing for more than one genetic condition: clinical and ethical considerations and dilemmas.
van der Schoot V et al. Human reproduction (Oxford, England) 2019 May - Points-to-consider on the return of results in epigenetic research.
Dyke Stephanie O M et al. Genome medicine 2019 May 11(1) 31 - Genomic testing in myeloid malignancy.
Docking T Roderick et al. International journal of laboratory hematology 2019 May 41 Suppl 1117-125 - Finding Out You Have a Genetic Mutation May Not Be as Bad as You Think- Scientists are learning they greatly overestimated chances of developing deadly cancers in patients with no family history of disease
M Cortez, Bloomberg News, May 9, 2019 - Inherited cardiomyopathies.
Miles Chris et al. BMJ (Clinical research ed.) 2019 05 l1570 - A Tale of Two Capacities: Including Children and Decisionally Vulnerable Adults in Biomedical Research.
Dalpé Gratien et al. Frontiers in genetics 2019 10289
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