Clinical and Genetic Heterogeneity of the 15q13.3 Microdeletion Syndrome

Por Hassfurther, Ariane, Komini, Eleni, Fischer, Judith, Leipoldt, Michael
Publicado no Mol Syndromol (2016)

Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans

Por Radner, Franz P. W., Marrakchi, Slaheddine, Kirchmeier, Peter, Kim, Gwang-Jin, Ribierre, Florence, Kamoun, Bourane, Abid, Leila, Leipoldt, Michael, Turki, Hamida, Schempp, Werner, Heilig, Roland, Lathrop, Mark, Fischer, Judith
Publicado em 2013

Correction: Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans

Por Radner, Franz P. W., Marrakchi, Slaheddine, Kirchmeier, Peter, Kim, Gwang-Jin, Ribierre, Florence, Kamoun, Bourane, Abid, Leila, Leipoldt, Michael, Turki, Hamida, Schempp, Werner, Heilig, Roland, Lathrop, Mark, Fischer, Judith
Publicado em 2013