Clinical Genomic Database

le Solomon, Benjamin D., Nguyen, Anh-Dao, Bear, Kelly A., Wolfsberg, Tyra G.
Foilsithe 2013

Evidence for SHH as a candidate gene for encephalocele

le Bear, Kelly A., Solomon, Benjamin D., Roessler, Erich, Pineda Alvarez, Daniel E., Kubendran, Shobana, O’Hara, Margaret, Muenke, Maximilian
Foilsithe 2012

Clinical Geneticists’ Views of VACTERL/VATER Association

le Solomon, Benjamin D., Bear, Kelly A., Kimonis, Virginia, de Klein, Annelies, Scott, Daryl A., Shaw-Smith, Charles, Tibboel, Dick, Reutter, Heiko, Giampietro, Philip F.
Foilsithe 2012

An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with eso...

le Solomon, Benjamin D., Baker, Linda A., Bear, Kelly A., Cunningham, Bridget K., Giampietro, Philip F., Hadigan, Colleen, Hadley, Donald W., Harrison, Steven, Levitt, Marc A., Niforatos, Nickie, Paul, Scott M., Raggio, Cathleen, Reutter, Heiko, Warren-Mora, Nicole
Foilsithe 2013

Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly

le Bear, Kelly A, Solomon, Benjamin D, Antonini, Sonir, Arnhold, Ivo J P, França, Marcela M, Gerkes, Erica H, Grange, Dorothy K, Hadley, Donald W, Jääskeläinen, Jarmo, Paulo, Sabrina S, Rump, Patrick, Stratakis, Constantine A, Thompson, Elizabeth M, Willis, Mary, Winder, Thomas L, Jorge, Alexander A L, Roessler, Erich, Muenke, Maximilian
Foilsithe in J Med Genet (2014)