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As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.Articles
Increased gestational palmitic acid predisposes offspring to congenital heart disease
Main text Congenital heart disease (CHD), which refers to a wide spectrum of structural malformations occurring in the heart, valves, and endothoracic great blood vessels during embryonic cardiogenesis, represents the most prevalent kind of human birth defect, with an estimated prevalence of 1% in newborns and up to 10% in stillbirths worldwide. 2 Tsao C.W. Aday A.W. Almarzooq Z.I. Alonso A. Beaton A.Z. Bittencourt M.S. Boehme A.K. Buxton A.E. Carson A.P. Commodore-Mensah Y. et al.
A SHOX2 loss-of-function mutation underlying familial atrial fibrillation
Global reach, higher impact Theranostics Journal of Cancer International Journal of Biological Sciences Journal of Genomics Nanotheranostics Oncomedicine Journal of Biomedicine Int J Med Sci 2018; 15(13):1564-1572.
TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus
TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus 1. Department of Cardiovascular Surgery, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, 1630 Dongfang Road, Shanghai 200127, China; 2. Department of Cardiovascular Medicine, East Hospital, Tongji University School of Medicine, 150 Jimo Road, Shanghai 200120, China; 3.
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