Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome

MLA

Vega, H., et al. “Phenotypic Variability in 49 Cases of ESCO2 Mutations, Including Novel Missense and Codon Deletion in the Acetyltransferase Domain, Correlates with ESCO2 Expression and Establishes the Clinical Criteria for Roberts Syndrome.” Vega , H , Trainer , A H , Gordillo , M , Crosier , M , Kayserili , H , Skovby , F , Uzielli , M L G , Schnur , R E , Manouvrier , S , Blair , E , Hurst , J A , Forzano , F , Meins , M , Simola , M K , Raas-Rothschild , A , Hennekam , R C M & Jabs , E W 2010 , ’ Phenotypic Variability in 49 Cases of ESCO2 Mutations, Including Novel Missense and Codon Deletion in the Acetyltransferase Domain, Correlates with ESCO2 Expression and Establishes the Clinical Criteria for Roberts Syndrome ’ , Journal of Medical Genetics , Vol. 47 , No. 1 , Pp. 30-7 , 2010. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1322607542&authtype=sso&custid=ns315887.

APA

Vega, H., Trainer, A. H., Gordillo, M., Crosier, M., Kayserili, H., Skovby, F., Uzielli, M. L. G., Schnur, R. E., Manouvrier, S., Blair, E., Hurst, J. A., Forzano, F., Meins, M., Simola, M. K., Raas-Rothschild, A., Hennekam, R. C. M., & Jabs, E. W. (2010). Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome. Vega , H , Trainer , A H , Gordillo , M , Crosier , M , Kayserili , H , Skovby , F , Uzielli , M L G , Schnur , R E , Manouvrier , S , Blair , E , Hurst , J A , Forzano , F , Meins , M , Simola , M K , Raas-Rothschild , A , Hennekam , R C M & Jabs , E W 2010 , ’ Phenotypic Variability in 49 Cases of ESCO2 Mutations, Including Novel Missense and Codon Deletion in the Acetyltransferase Domain, Correlates with ESCO2 Expression and Establishes the Clinical Criteria for Roberts Syndrome ’ , Journal of Medical Genetics , Vol. 47 , No. 1 , Pp. 30-7 .

Chicago

Vega, H, A H Trainer, M Gordillo, M Crosier, H Kayserili, F Skovby, M L Giovannucci Uzielli, et al. 2010. “Phenotypic Variability in 49 Cases of ESCO2 Mutations, Including Novel Missense and Codon Deletion in the Acetyltransferase Domain, Correlates with ESCO2 Expression and Establishes the Clinical Criteria for Roberts Syndrome.” Vega , H , Trainer , A H , Gordillo , M , Crosier , M , Kayserili , H , Skovby , F , Uzielli , M L G , Schnur , R E , Manouvrier , S , Blair , E , Hurst , J A , Forzano , F , Meins , M , Simola , M K , Raas-Rothschild , A , Hennekam , R C M & Jabs , E W 2010 , ’ Phenotypic Variability in 49 Cases of ESCO2 Mutations, Including Novel Missense and Codon Deletion in the Acetyltransferase Domain, Correlates with ESCO2 Expression and Establishes the Clinical Criteria for Roberts Syndrome ’ , Journal of Medical Genetics , Vol. 47 , No. 1 , Pp. 30-7 . http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1322607542&authtype=sso&custid=ns315887.