“Molecular rulers” for calibrating phenotypic effects of telomere imbalance von Martin, C L, Waggoner, D J, Wong, A, Uhrig, S, Roseberry, J A, Hedrick, J F, Pack, S D, Russell, K, Zackai, E, Dobyns, W B, Ledbetter, D H

Volltext

The Role of Copper in Neurodegenerative Disease von Waggoner, Darrel J., Bartnikas, Thomas B., Gitlin, Jonathan D.

Volltext

Identification of Novel Adhesins from Group B Streptococci by Use of Phage Display Reveals that C5a Peptidase Mediates Fibronectin Binding von BECKMANN, Christiane, WAGGONER, Joshua D, HARRIS, Theresa O, TAMURA, Glen S, RUBENS, Craig E

Volltext

Brain Copper Content and Cuproenzyme Activity Do Not Vary with Prion Protein Expression Level von Waggoner, Darrel J., Drisaldi, Bettina, Bartnikas, Thomas B., Casareno, Ruby Leah B., Prohaska, Joseph R., Gitlin, Jonathan D., Harris, David A.

Volltext

Integration of internet-based genetic databases into the medical school pre-clinical and clinical curriculum von Waggoner, Darrel J, Martin, Christa Lese

Volltext

Vertebral anomalies in a new family with ODED syndrome von Piersall, Linda D, Dowton, S Bruce, McAlister, William H, Waggoner, Darrel J

Volltext

Clinic-based study of plexiform neurofibromas in neurofibromatosis 1 von Waggoner, Darrel J., Towbin, Jennifer, Gottesman, Gary, Gutmann, David H.

Volltext

Armenian hamster female protein (serum amyloid P component). Comparison with the sex-regulated homolog in Syrian hamster von Dowton, SB, Waggoner, DJ

Volltext

Developmental regulation of expression of C-reactive protein and serum amyloid A in Syrian hamsters von DOWTON, S. B, WAGGONER, D. J, MANDL, K. D

Volltext

Chromosomal localization of CCS, the copper chaperone for Cu/Zn superoxide dismutase von Bartnikas, T B, Waggoner, D J, Casareno, R L, Gaedigk, R, White, R A, Gitlin, J D

Volltext

TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome von MCDERMOTT, Deborah A, BRESSAN, Michael C, PIERPONT, Mary Ella, RAAS-ROTHSCHILD, Annick, SHANSKE, Alan L, SMITH, Wendy E, SPENCER, Robert H, JOHN-SUTTON, Martin G. St, VAN MALDERGEM, Lionel, WAGGONER, Darrel J, WEBER, Matthew, BASSON, Craig T, JIE HE, LEE, Joseph S, AFTIMOS, Salim, BRUECKNER, Martina, GILBERT, Fred, GRAHAM, Gail E, HANNIBAL, Mark C, INNIS, Jeffrey W

Volltext

Methylmalonic aciduria (cblF): Case report and response to therapy von Waggoner, D.J., Ueda, K., Mantia, C., Dowton, S.B.

Volltext

Partial monosomy of distal 10q: Three new cases and a review von Waggoner, Darrel J., Chow, Clara K., Dowton, S. Bruce, Watson, Michael S.

Volltext

Parents: Critical Stakeholders in Expanding Newborn Screening von Ross, Lainie Friedman, MD, PhD, Waggoner, Darrel J., MD

Volltext

Deletion of 1q in a patient with acrofacial dysostosis von Waggoner, Darrel J., Ciske, David J., Dowton, S. Bruce, Watson, Michael S.

Volltext

NSD1 analysis for Sotos syndrome: Insights and perspectives from the clinical laboratory von Waggoner, Darrel J., Raca, Gordana, Welch, Katherine, Dempsey, Melissa, Anderes, Ethan, Ostrovnaya, Irina, Alkhateeb, Asem, Kamimura, Junichi, Matsumoto, Naomichi, Schaeffer, G Bradley, Martin, Christa Lese, Das, Soma

Volltext

Unique cardiac and cerebral anomalies with chondrodysplasia punctata von Ciske, David J., Waggoner, Darrel J., Dowton, S. Bruce

Volltext

Familial Pyloric Stenosis Associated with Developmental Delays von Elinoff, Jason M, Liu, Donald, Guandalini, Stefano, Waggoner, Darrel J

Volltext

Identification of Novel Adhesins from Group B Streptococci by Use of Phage Display Reveals that C5a Peptidase Mediates Fibronectin Binding von Beckmann, Christiane, Waggoner, Joshua D., Harris, Theresa O., Tamura, Glen S., Rubens, Craig E.

Volltext

Letters von Waggoner, J. D.

Volltext