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10.1159/000445788 http://scihub22266oqcxt.onion/10.1159/000445788 C4906429!4906429!27385961     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Mol+Syndromol 2016 ; 7 (2): 51-61 Nephropedia Template TP {{tp|p=27385961|t=2016. Cytogenomic Aberrations in Congenital Cardiovascular Malformations |pdf=|usr=}}{{27385961}} gab.com Text Cytogenomic Aberrations in Congenital Cardiovascular Malformations JO: Mol Syndromol http://www.kidney.de/pget.php?&tw=1&pmid=27385961 #FOAvip Congenital cardiovascular malformations are the most common birth defects, with a complex multifactorial etiology. Genetic factors play an important role, illuminated by numerous cytogenetically visible abnormalities, as well as submicroscopic genomic imbalances affecting critical genomic regions in the affected individuals. Study of rare families with Mendelian forms, as well as emerging next-generation sequencing technologies have uncovered a multitude of genes relevant for human congenital cardiac diseases. It is clear that the complex embryology of human cardiac development, with an orchestrated interplay of transcription factors, chromatin regulators, and signal transduction pathway molecules can be easily perturbed by genomic imbalances affecting dosage-sensitive regions. This review focuses on chromosomal abnormalities contributing to congenital heart diseases and underscores several genomic disorders linked to human cardiac malformations in the last few decades. Twit Text FOAVip Cytogenomic Aberrations in Congenital Cardiovascular Malformations ????Mol Syndromol http://www.kidney.de/pget.php?&tw=1&pmid=27385961 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27385961 #FOAvip English Wikipedia <ref>{{Cite pmid|27385961}}</ref> Cytogenomic Aberrations in Congenital Cardiovascular Malformations #MMPMID27385961 Azamian M; Lalani SR Mol Syndromol 2016[May]; 7 (2): 51-61 PMID27385961show ga Congenital cardiovascular malformations are the most common birth defects, with a complex multifactorial etiology. Genetic factors play an important role, illuminated by numerous cytogenetically visible abnormalities, as well as submicroscopic genomic imbalances affecting critical genomic regions in the affected individuals. Study of rare families with Mendelian forms, as well as emerging next-generation sequencing technologies have uncovered a multitude of genes relevant for human congenital cardiac diseases. It is clear that the complex embryology of human cardiac development, with an orchestrated interplay of transcription factors, chromatin regulators, and signal transduction pathway molecules can be easily perturbed by genomic imbalances affecting dosage-sensitive regions. This review focuses on chromosomal abnormalities contributing to congenital heart diseases and underscores several genomic disorders linked to human cardiac malformations in the last few decades. äCytogenomic Aberrations in Congenital Cardiovascular Malformations (epmc).pdf DeepDyve Pubget Overpricing