Phenotypic features of carbohydrate sulfotransferase 3 (CHST3) deficiency in 24 patients: congenital dislocations and vertebral changes as principal diagnostic features

MLA

Bernhard Zabel, et al. “Phenotypic Features of Carbohydrate Sulfotransferase 3 (CHST3) Deficiency in 24 Patients: Congenital Dislocations and Vertebral Changes as Principal Diagnostic Features.” American Journal of Medical Genetics. Part A, no. 10, Sept. 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=edsair&AN=edsair.doi.dedup.....0f4c55d19c86a38f907c95f917acebff&authtype=sso&custid=ns315887.

APA

Bernhard Zabel, Julia Hoefele, Emma Wakeling, Luisa Bonafé, Roberto Mendoza-Londono, Nithiwat Vatanavicharn, Sheela Nampoothiri, Imma Rost, Melanie Alcausin, Sophia Hollander, Bryan D. Hall, Elisabeth Mangold, J. Spranger, Ekkehart Lausch, Andrea Superti-Furga, Stephen Ts Lam, Kerstin Reicherter, Sheila Unger, David Sillence, … Antonio Aytes. (2010). Phenotypic features of carbohydrate sulfotransferase 3 (CHST3) deficiency in 24 patients: congenital dislocations and vertebral changes as principal diagnostic features. American Journal of Medical Genetics. Part A, 10.

Chicago

Bernhard Zabel, Julia Hoefele, Emma Wakeling, Luisa Bonafé, Roberto Mendoza-Londono, Nithiwat Vatanavicharn, Sheela Nampoothiri, et al. 2010. “Phenotypic Features of Carbohydrate Sulfotransferase 3 (CHST3) Deficiency in 24 Patients: Congenital Dislocations and Vertebral Changes as Principal Diagnostic Features.” American Journal of Medical Genetics. Part A, no. 10 (September). 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=edsair&AN=edsair.doi.dedup.....0f4c55d19c86a38f907c95f917acebff&authtype=sso&custid=ns315887.