Null mutation of endothelin receptor type B gene in spotting lethal rats causes aganglionic megacolon and white coat color.

por Gariepy, C E, Cass, D T, Yanagisawa, M
Publicado 1996

Congenital central hypoventilation syndrome and Hirschsprung's disease

por Croaker, G, Shi, E, Simpson, E, Cartmill, T, Cass, D
Publicado 1998

Better To Be Safe than “Sarry”: Preparing for Severe Acute Respiratory Syndrome

por Berriel-Cass∗, D., Gorczyca, J., Roth, L.A., DeSantis, L., Fakih, M.
Publicado en Am J Infect Control (2004)

MNGIE with lack of skeletal muscle involvement and a novel TP splice site mutation

por Szigeti, K, Wong, L, Perng, C, Saifi, G, Eldin, K, Adesina, A, Cass, D, Hirano, M, Lupski, J, Scaglia, F
Publicado 2004

Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23.

por Mowat, D R, Croaker, G D, Cass, D T, Kerr, B A, Chaitow, J, Adès, L C, Chia, N L, Wilson, M J
Publicado 1998