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10.1097/MCD.0b013e32833ff29d http://scihub22266oqcxt.onion/10.1097/MCD.0b013e32833ff29d 21178588!ä!21178588 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       Clin+Dysmorphol 2011 ; 20 (2): 86-88 Nephropedia Template TP {{tp|p=21178588|t=2011. Cardiofaciocutaneous syndrome in a mother and two sons with a MEK2 mutation |pdf=|usr=}}{{21178588}} gab.com Text Cardiofaciocutaneous syndrome in a mother and two sons with a MEK2 mutation JO: Clin Dysmorphol http://www.kidney.de/pget.php?&tw=1&pmid=21178588 #FOAvip ä Twit Text FOAVip Cardiofaciocutaneous syndrome in a mother and two sons with a MEK2 mutation ????Clin Dysmorphol http://www.kidney.de/pget.php?&tw=1&pmid=21178588 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=21178588 #FOAvip English Wikipedia <ref>{{Cite pmid|21178588}}</ref> Cardiofaciocutaneous syndrome in a mother and two sons with a MEK2 mutation #MMPMID21178588 Linden HC; Price SM Clin Dysmorphol 2011[Apr]; 20 (2): 86-88 PMID21178588show ga ä |Adult[MESH] |Adult Children[MESH] |Aged[MESH] |Ectodermal Dysplasia/diagnosis[MESH] |Facies[MESH] |Failure to Thrive/diagnosis[MESH] |Female[MESH] |Heart Defects, Congenital/diagnosis[MESH] |Heredity[MESH] |Humans[MESH] |Keratoderma, Palmoplantar/diagnosis/genetics[MESH] |Lentigo/congenital/diagnosis[MESH] |MAP Kinase Kinase 2/*genetics[MESH] |Male[MESH] |Middle Aged[MESH] |Mothers[MESH] |Mutation, Missense[MESH] |Myopia/congenital/diagnosis[MESH] |Pedigree[MESH] |Polyhydramnios/diagnosis[MESH] |Pregnancy[MESH]Cardiofaciocutaneous syndrome in a mother and two sons with a MEK2 mut(epmc).pdf DeepDyve Pubget Overpricing