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

CDC/NIH Web Information Database|Home|PHGKB

CDC/NIH Web Information Database


CDC/NIH Information Database|Search|PHGKB

Last data update: Dec 01, 2023. (Total: 8775 Documents)
   dataset      
Next
Records 1-30 (of 32 Records)
CDC/NIH Web Information
The Use of Cell-free DNA in Clinical Practice: Work in Progress
M Clyne et al, CDC Blog Post, December 14, 2022 Brand
Hypertrophic Cardiomyopathy and Public Health: An Expanding List of Tier 1 Genomic Applications
CDC Seminar Announcement, January 27, 2022 Brand
New CDC Partnerships to Advance the Development and Validation of Next Generation Sequencing Tests: A Publicly Available List of Expert Curated Variants
L Kalman et al, CDC Blog Post, November 16, 2021 Brand
An Expanding List of Tier 1 Genomic Applications: Evidence-based Guidelines for Hypertrophic Cardiomyopathy and Public Health
MA Burke et al, CDC Blog, October 6,2021 Brand
Modeling Hypertrophic Cardiomyopathy in a Dish
NIH Director's Blog, November 8, 2018 Brand
Cardiomyopathy represents a collection of diverse conditions of the heart muscle
Brand
Angina
From NHLBI health topic site Brand
Cardiomyopathy
From NHLBI health topic site Brand
Diabetic Heart Disease
From NHLBI health topic site Brand
Heart Disease in Women
From NHLBI health topic site Brand
Heart Palpitations
From NHLBI health topic site Brand
Peripartum cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Dilated cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy cataract hip spine disease
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy diabetes deafness
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy dilated with conduction defect type 1
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy due to anthracyclines
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy and deafness due to tRNA lysine gene mutation
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy hypogonadism metabolic anomalies
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy spherocytosis
From NCATS Genetic and Rare Diseases Information Center Brand
Hypogonadism cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Familial dilated cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Dilated cardiomyopathy with hypergonadotropic hypogonadism
From NCATS Genetic and Rare Diseases Information Center Brand
Microcephaly-cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Spine rigid cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy dilated with woolly hair and keratoderma
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy dilated with conduction defect type 2
From NCATS Genetic and Rare Diseases Information Center Brand
Doxorubicin induced cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Familial hypertrophic cardiomyopathy
From NCATS Genetic and Rare Diseases Information Center Brand
Cardiomyopathy, fatal fetal, due to myocardial calcification
From NCATS Genetic and Rare Diseases Information Center Brand
TOP