Dysregulation of Chondrogenesis in Human Cleidocranial Dysplasia

door Zheng, Qiping, Sebald, Eiman, Zhou, Guang, Chen, Yuqing, Wilcox, William, Lee, Brendan, Krakow, Deborah
Gepubliceerd in 2005

Dominance of SOX9 function over RUNX2 during skeletogenesis

door Zhou, Guang, Zheng, Qiping, Engin, Feyza, Munivez, Elda, Chen, Yuqing, Sebald, Eiman, Krakow, Deborah, Lee, Brendan
Gepubliceerd in 2006

GDF5 Is a Second Locus for Multiple-Synostosis Syndrome

door Dawson, Katherine, Seeman, Petra, Sebald, Eiman, King, Lily, Edwards, Matthew, Williams III, John, Mundlos, Stephan, Krakow, Deborah
Gepubliceerd in 2006

Type XXVII collagen at the transition of cartilage to bone during skeletogenesis

door Hjorten, Rebecca, Hansen, Uwe, Underwood, Robert A., Telfer, Helena E., Fernandes, Russell J., Krakow, Deborah, Sebald, Eiman, Wachsmann-Hogiu, Sebastian, Bruckner, Peter, Jacquet, Robin, Landis, William J., Byers, Peter H., Pace, James M.
Gepubliceerd in 2007

Ciliary Abnormalities Due to Defects in the Retrograde Transport Protein DYNC2H1 in Short-Rib Polydactyly Syndrome

door Merrill, Amy E., Merriman, Barry, Farrington-Rock, Claire, Camacho, Natalia, Sebald, Eiman T., Funari, Vincent A., Schibler, Matthew J., Firestein, Marc H., Cohn, Zachary A., Priore, Mary Ann, Thompson, Alicia K., Rimoin, David L., Nelson, Stanley F., Cohn, Daniel H., Krakow, Deborah
Gepubliceerd in 2009