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American Journal of Human Genetics|June 13, 1998
Paternal uniparental disomy for chromosome 1 revealed by molecular analysis of a patient with pycnodysostosisB D Gelb, J P Willner, T M Dunn, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 7, 2006
Mice lacking cathepsin K maintain bone remodeling but develop bone fragility despite high bone massChao Yang Li, Karl J Jepsen, Robert J Majeska, et al.
American Journal of Medical Genetics. Part A|June 9, 2005
PTPN11 mutations play a minor role in isolated congenital heart diseaseConstance G Weismann, A Hager, H Kaemmerer, et al.
The American Journal of Cardiology|September 2, 1998
Usefulness of tacrolimus versus cyclosporine after pediatric heart transplantationG Z Herzberg, A F Rossi, M Courtney, et al.
Nature Genetics|May 10, 2000
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosusM Satoda, F Zhao, G A Diaz, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|July 15, 2014
Pediatric cardiac retransplantation: Waitlist mortality stratified by age and eraMatthew J Bock, Khanh Nguyen, Stefano Malerba, et al.
Experimental Biology and Medicine (Maywood, N.J.)|May 14, 2010
Ash2l interacts with Tbx1 and is required during early embryogenesisJason Z Stoller, Li Huang, Cheryl C Tan, et al.
Human Molecular Genetics|July 29, 2016
SHOC2 subcellular shuttling requires the KEKE motif-rich region and N-terminal leucine-rich repeat domain and impacts on ERK signallingMarialetizia Motta, Giovanni Chillemi, Valentina Fodale, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 26, 1999
Determination of bone markers in pycnodysostosis: effects of cathepsin K deficiency on bone matrix degradationY Nishi, L Atley, D E Eyre, et al.
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