Capecitabine-Induced Enterocolitis

por Khan, Muzammil, Kleyner, Robert, Abbasi, Sadia, Haider, Asim
Publicado 2022

KBG syndrome involving a single-nucleotide duplication in ANKRD11

por Kleyner, Robert, Malcolmson, Janet, Tegay, David, Ward, Kenneth, Maughan, Annette, Maughan, Glenn, Nelson, Lesa, Wang, Kai, Robison, Reid, Lyon, Gholson J.
Publicado 2016

Autosomal recessive SLC30A9 variants in a proband with a cerebrorenal syndrome and no parental consanguinity

por Kleyner, Robert, Arif, Mohammad, Marchi, Elaine, Horowitz, Naomi, Haworth, Andrea, King, Brian, Gavin, Maureen, Amble, Karen, Velinov, Milen, Lyon, Gholson J.
Publicado 2022

SCN8A mutation in a child presenting with seizures and developmental delays

por Malcolmson, Janet, Kleyner, Robert, Tegay, David, Adams, Whit, Ward, Kenneth, Coppinger, Justine, Nelson, Lesa, Meisler, Miriam H., Wang, Kai, Robison, Reid, Lyon, Gholson J.
Publicado 2016