Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText. Kick-your-searchterm to multiple Engines kick-your-query now !>

A dictionary by aggregated review articles of nephrology, medicine and the life sciences Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

10.1161/CIRCRESAHA.116.309140 http://scihub22266oqcxt.onion/10.1161/CIRCRESAHA.116.309140 C5557504!5557504!28302740     free     free     free       Circ+Res 2017 ; 120 (6): 923-40 Nephropedia Template TP {{tp|p=28302740|t=2017. Genetics and Genomics of Congenital Heart Disease |pdf=|usr=}}{{28302740}} gab.com Text Genetics and Genomics of Congenital Heart Disease JO: Circ Res http://www.kidney.de/pget.php?&tw=1&pmid=28302740 #FOAvip Congenital heart disease is the most common birth defect, and due to major advances in medical and surgical management, there are now more adults living with CHD than children. Until recently, the cause of the majority of CHD was unknown. Advances in genomic technologies have discovered the genetic etiology of a significant fraction of CHD, while at the same time pointing to remarkable complexity in CHD genetics. This review will focus on the evidence for genetic causes underlying CHD and discuss data supporting both monogenic and complex genetic mechanisms underlying CHD. The discoveries from CHD genetic studies draw attention to biological pathways that simultaneously open the door to a better understanding of cardiac development, and impact clinical care of CHD patients. Finally, we address clinical genetic evaluation of patients and families affected by CHD. Twit Text FOAVip Genetics and Genomics of Congenital Heart Disease ????Circ Res http://www.kidney.de/pget.php?&tw=1&pmid=28302740 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28302740 #FOAvip English Wikipedia <ref>{{Cite pmid|28302740}}</ref> Genetics and Genomics of Congenital Heart Disease #MMPMID28302740 Zaidi S; Brueckner M Circ Res 2017[Mar]; 120 (6): 923-40 PMID28302740show ga Congenital heart disease is the most common birth defect, and due to major advances in medical and surgical management, there are now more adults living with CHD than children. Until recently, the cause of the majority of CHD was unknown. Advances in genomic technologies have discovered the genetic etiology of a significant fraction of CHD, while at the same time pointing to remarkable complexity in CHD genetics. This review will focus on the evidence for genetic causes underlying CHD and discuss data supporting both monogenic and complex genetic mechanisms underlying CHD. The discoveries from CHD genetic studies draw attention to biological pathways that simultaneously open the door to a better understanding of cardiac development, and impact clinical care of CHD patients. Finally, we address clinical genetic evaluation of patients and families affected by CHD. äGenetics and Genomics of Congenital Heart Disease (epmc).pdf DeepDyve Pubget Overpricing