Last Posted: Nov 14, 2019
- Confidential genetic testing and electronic health records: A survey of current practices among Huntington disease testing centers.
Eno Celeste C et al. Molecular genetics & genomic medicine 2019 Nov e1026 - Fragile X syndrome carrier screening accompanied by genetic consultation has clinical utility in populations beyond those recommended by guidelines.
Johansen Taber Katherine et al. Molecular genetics & genomic medicine 2019 Nov e1024 - Era of Genomic Medicine: A Narrative Review on CRISPR Technology as a Potential Therapeutic Tool for Human Diseases.
Kotagama Odatha W et al. BioMed research international 2019 20191369682 - Current Policy Challenges in Genomic Medicine
RD Klein, Clinical Chemistry, November 2019 - New genetic analysis improves diagnosis of intellectual disability
Karolinska Institute, November 11, 2019 - Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project.
Sanderson Saskia C et al. BMJ open 2019 Nov (11) e029699 - UVM Health Network to offer DNA testing as part of primary care
K Jickling, Support VTDigger, November 7,y 2019 - Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years' experience in Catalonia (Spain).
Martin-Nalda Andrea et al. Molecular genetics & genomic medicine 2019 Oct e1016 - Genomic Medicine XII: Genomics and Risk Prediction
NHGRI 2019 meeting and slide presentations - [Genomic medicine in public health policies: a perspective of Mexican biomedical researchers].
Oliva-Sánchez Pablo Francisco et al. Salud publica de Mexico 55(1) 16-25
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