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10.1002/ajmg.a.37881 http://scihub22266oqcxt.onion/10.1002/ajmg.a.37881 C5930355!5930355!27518916     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 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Am+J+Med+Genet+A 2016 ; 170 (9): 2261-4 Nephropedia Template TP {{tp|p=27518916|t=2016. Tumor Screening in Beckwith-Wiedemann Syndrome ? To Screen or Not to Screen?|pdf=|usr=}}{{27518916}} gab.com Text Tumor Screening in Beckwith-Wiedemann Syndrome To Screen or Not to Screen JO: Am J Med Genet A http://www.kidney.de/pget.php?&tw=1&pmid=27518916 #FOAvip Beckwith-Wiedemann syndrome (BWS) is the most common imprinting disorder and consequently, one of the most common cancer predisposition disorders. Over the past 20 years, our understanding of the genetics and epigenetics leading to BWS has evolved and genotype/phenotype correlations have become readily apparent. Clinical management of these patients is focused on omphaloceles, hypoglycemia, macroglossia, hemihypertrophy, and tumor screening. Until recently, the need for tumor screening has been thought to be largely uniform across all genetic and epigenetic causes of BWS. As tumor risk correlates with genetic and epigenetic causes of BWS, several groups have proposed alterations to tumor screening protocols based on the etiology of BWS. However, there are many challenges inherent in adapting screening protocols. Such protocols must accommodate not only the risk based on genetic and epigenetic causes but also the medical cost-benefit of screening, the psychological impact on families, and the social-legal implications of missing a treatable tumor. Twit Text FOAVip Tumor Screening in Beckwith-Wiedemann Syndrome To Screen or Not to Screen ????Am J Med Genet A http://www.kidney.de/pget.php?&tw=1&pmid=27518916 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27518916 #FOAvip English Wikipedia <ref>{{Cite pmid|27518916}}</ref> Tumor Screening in Beckwith-Wiedemann Syndrome ? To Screen or Not to Screen? #MMPMID27518916 Kalish JM; Deardorff MA Am J Med Genet A 2016[Sep]; 170 (9): 2261-4 PMID27518916show ga Beckwith-Wiedemann syndrome (BWS) is the most common imprinting disorder and consequently, one of the most common cancer predisposition disorders. Over the past 20 years, our understanding of the genetics and epigenetics leading to BWS has evolved and genotype/phenotype correlations have become readily apparent. Clinical management of these patients is focused on omphaloceles, hypoglycemia, macroglossia, hemihypertrophy, and tumor screening. Until recently, the need for tumor screening has been thought to be largely uniform across all genetic and epigenetic causes of BWS. As tumor risk correlates with genetic and epigenetic causes of BWS, several groups have proposed alterations to tumor screening protocols based on the etiology of BWS. However, there are many challenges inherent in adapting screening protocols. Such protocols must accommodate not only the risk based on genetic and epigenetic causes but also the medical cost-benefit of screening, the psychological impact on families, and the social-legal implications of missing a treatable tumor. äTumor Screening in Beckwith-Wiedemann Syndrome ? To Screen or Not to S(epmc).pdf DeepDyve Pubget Overpricing