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10.1007/s40142-014-0052-8 http://scihub22266oqcxt.onion/10.1007/s40142-014-0052-8 C4226515!4226515!25396100     free     free     free Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\25396100.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Curr+Genet+Med+Rep 2014 ; 2 (4): 212-5 Nephropedia Template TP {{tp|p=25396100|t=2014. Clinical Management of Pediatric Genomic Testing |pdf=|usr=}}{{25396100}} gab.com Text Clinical Management of Pediatric Genomic Testing JO: Curr Genet Med Rep http://www.kidney.de/pget.php?&tw=1&pmid=25396100 #FOAvip As sequencing becomes integrated into clinical medicine, many complex ethical questions arise regarding the return of genomic information, especially in pediatrics. Issues center on the best interests of the child, particularly in return of information about adult-onset conditions. These include the child's future autonomous decision-making and access to knowledge about treatable conditions, the child in the family unit, and benefit to family members of learning information which could impact them personally. This article first discusses the framework for returning genomic information, and then ethical issues regarding return of results. Finally it discusses potential harms and benefits, while recognizing that little is known about what these actually are. A new era of genomic information is in its infancy; handling genomic information in a way that provides patients and their families with knowledge that is helpful without causing distress is the greatest challenge. Twit Text FOAVip Clinical Management of Pediatric Genomic Testing ????Curr Genet Med Rep http://www.kidney.de/pget.php?&tw=1&pmid=25396100 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25396100 #FOAvip English Wikipedia <ref>{{Cite pmid|25396100}}</ref> Clinical Management of Pediatric Genomic Testing #MMPMID25396100 Holm IA Curr Genet Med Rep 2014[Dec]; 2 (4): 212-5 PMID25396100show ga As sequencing becomes integrated into clinical medicine, many complex ethical questions arise regarding the return of genomic information, especially in pediatrics. Issues center on the best interests of the child, particularly in return of information about adult-onset conditions. These include the child's future autonomous decision-making and access to knowledge about treatable conditions, the child in the family unit, and benefit to family members of learning information which could impact them personally. This article first discusses the framework for returning genomic information, and then ethical issues regarding return of results. Finally it discusses potential harms and benefits, while recognizing that little is known about what these actually are. A new era of genomic information is in its infancy; handling genomic information in a way that provides patients and their families with knowledge that is helpful without causing distress is the greatest challenge. äClinical Management of Pediatric Genomic Testing (epmc).pdf DeepDyve Pubget Overpricing