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10.1159/000437061 http://scihub22266oqcxt.onion/10.1159/000437061 C4698645!4698645!26732610     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26732610&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 247.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 247.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Mol+Syndromol 2015 ; 6 (3): 147-51 Nephropedia Template TP {{tp|p=26732610|t=2015. Familial 1 3-Mb 11p15 5p15 4 Duplication in Three Generations Causing Silver-Russell and Beckwith-Wiedemann Syndromes |pdf=|usr=}}{{26732610}} gab.com Text Familial 1 3-Mb 11p15 5p15 4 Duplication in Three Generations Causing Silver-Russell and Beckwith-Wiedemann Syndromes JO: Mol Syndromol http://www.kidney.de/pget.php?&tw=1&pmid=26732610 #FOAvip Silver-Russell syndrome (SRS) and Beckwith-Wiedemann syndrome (BWS) are 2 opposite growth-affecting disorders. The common molecular cause for both syndromes is an abnormal regulation of genes in chromosomal region 11p15, where 2 imprinting control regions (ICR) control fetal and postnatal growth. Also, many submicroscopic chromosomal disturbances like duplications in 11p15 have been described among SRS and BWS patients. Duplications involving both ICRs cause SRS or BWS, depending on which parent the aberration is inherited from. We describe to our knowledge the smallest familial pure 1.3-Mb duplication in chromosomal region 11p15.5p15.4 that involves both ICRs and is present in 3 generations causing an SRS or BWS phenotype. Twit Text FOAVip Familial 1 3-Mb 11p15 5p15 4 Duplication in Three Generations Causing Silver-Russell and Beckwith-Wiedemann Syndromes ????Mol Syndromol http://www.kidney.de/pget.php?&tw=1&pmid=26732610 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26732610 #FOAvip English Wikipedia <ref>{{Cite pmid|26732610}}</ref> Familial 1 3-Mb 11p15 5p15 4 Duplication in Three Generations Causing Silver-Russell and Beckwith-Wiedemann Syndromes #MMPMID26732610 Vals MA; Kahre T; Mee P; Muru K; Kallas E; ?ilina O; Tillmann V; Õunap K Mol Syndromol 2015[Sep]; 6 (3): 147-51 PMID26732610show ga Silver-Russell syndrome (SRS) and Beckwith-Wiedemann syndrome (BWS) are 2 opposite growth-affecting disorders. The common molecular cause for both syndromes is an abnormal regulation of genes in chromosomal region 11p15, where 2 imprinting control regions (ICR) control fetal and postnatal growth. Also, many submicroscopic chromosomal disturbances like duplications in 11p15 have been described among SRS and BWS patients. Duplications involving both ICRs cause SRS or BWS, depending on which parent the aberration is inherited from. We describe to our knowledge the smallest familial pure 1.3-Mb duplication in chromosomal region 11p15.5p15.4 that involves both ICRs and is present in 3 generations causing an SRS or BWS phenotype. äFamilial 1 3-Mb 11p15 5p15 4 Duplication in Three Generations Causing (epmc).pdf DeepDyve Pubget Overpricing