Last Posted: Dec 19, 2019
- Re-analysis of whole-exome sequencing data uncovers novel diagnostic variants and improves molecular diagnostic yields for sudden death and idiopathic diseases.
Salfati Elias L et al. Genome medicine 2019 Dec (1) 83 - Rare Risk: Newly identified gene variants linked to increased risk for sudden cardiac death
Harvard Medical School, November 2019 - Hypertrophic cardiomyopathy: genetics and clinical perspectives.
Wolf Cordula Maria et al. Cardiovascular diagnosis and therapy 2019 Oct 9(Suppl 2) S388-S415 - Predicting Risk for Adult-Onset Sudden Cardiac Death in the Population
CR Bezzina et al, JACC, November 16, 2019 - Rare Genetic Variants Associated With Sudden Cardiac Death in Adults
AV Khera et al, JACC, November 2019 - Left ventricular noncompaction - Risk stratification and genetic consideration.
Ichida Fukiko et al. Journal of cardiology 2019 Oct - Learn What CDC Is Doing About Sudden Unexpected Infant Death (SUID)
CDC, 2019 - Genetics of Unexplained Sudden Cardiac Death in Adult Caucasian and African American Individuals Living in the State of Maryland
L Guo et al, MedRXIV, September 24, 2019 - The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy.
Lahrouchi Najim et al. European journal of human genetics : EJHG 2019 Sep - Clinical and ECG variables to predict the outcome of genetic testing in hypertrophic cardiomyopathy.
Robyns Tomas et al. European journal of medical genetics 2019 Sep 103754
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