Body mass index variation in adults with Williams syndrome: associations with predicted dietary intake and food behaviors

por Renzi, Danielle, Stanley, Takara, Waxler, Jessica, Lee, Hang, Pober, Barbara, Nordstrom, Marianne
Publicado 2023

Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia

por Chen, Haijun, von Hehn, Christian, Kaczmarek, Leonard K., Ment, Laura R., Pober, Barbara R., Hisama, Fuki M.
Publicado 2006

Fog2 Is Required for Normal Diaphragm and Lung Development in Mice and Humans

por Ackerman, Kate G, Herron, Bruce J, Vargas, Sara O, Huang, Hailu, Tevosian, Sergei G, Kochilas, Lazaros, Rao, Cherie, Pober, Barbara R, Babiuk, Randal P, Epstein, Jonathan A, Greer, John J, Beier, David R
Publicado 2005

Control of bone formation by the serpentine receptor Frizzled-9

por Albers, Joachim, Schulze, Jochen, Beil, F. Timo, Gebauer, Matthias, Baranowsky, Anke, Keller, Johannes, Marshall, Robert P., Wintges, Kristofer, Friedrich, Felix W., Priemel, Matthias, Schilling, Arndt F., Rueger, Johannes M., Cornils, Kerstin, Fehse, Boris, Streichert, Thomas, Sauter, Guido, Jakob, Franz, Insogna, Karl L., Pober, Barbara, Knobeloch, Klaus-Peter, Francke, Uta, Amling, Michael, Schinke, Thorsten
Publicado 2011

Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes

por Twigg, Stephen R.F., Babbs, Christian, van den Elzen, Marijke E.P., Goriely, Anne, Taylor, Stephen, McGowan, Simon J., Giannoulatou, Eleni, Lonie, Lorne, Ragoussis, Jiannis, Akha, Elham Sadighi, Knight, Samantha J.L., Zechi-Ceide, Roseli M., Hoogeboom, Jeannette A.M., Pober, Barbara R., Toriello, Helga V., Wall, Steven A., Rita Passos-Bueno, M., Brunner, Han G., Mathijssen, Irene M.J., Wilkie, Andrew O.M.
Publicado 2013