Human myelomeningocele risk and ultra-rare deleterious variants in genes associated with cilium, WNT-signaling, ECM, cytoskeleton and cell migration von Au, K. S., Hebert, L., Hillman, P., Baker, C., Brown, M. R., Kim, D.-K., Soldano, K., Garrett, M., Ashley-Koch, A., Lee, S., Gleeson, J., Hixson, J. E., Morrison, A. C., Northrup, H.

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Exploring the Substitution of Exenatide for Insulin in Patients With Type 2 Diabetes Treated With Insulin in Combination With Oral Antidiabetes Agents von Davis, Stephen N, Johns, Don, Maggs, David, Xu, Hangtao, Northrup, Justin H, Brodows, Robert G

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P.29 Case report: high protein requirements in maternal phenylketonuria von Roberts, P, Northrup, H

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Kinetics of Protein-Protein Association Explained by Brownian Dynamics Computer Simulation von Northrup, Scott H., Erickson, H. P.

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Contribution of Electrostatics to the Kinetics of Electron Transfer from NADH-Cytochrome b5 Reductase to Fe(III)-Cytochrome b5 von Kollipara, Sireesha, Tatireddy, Shivakishore, Pathirathne, Thusitha, Rathnayake, Lasantha K, Northrup, Scott H

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Efficacy and safety of the recommended pegvaliase dosing regimen in adults with phenylketonuria in the phase 3 PRISM studies von Lindstrom, K, Sacharow, S, Northrup, H, Whitehall, KB, Rowell, R, Burton, B, Thomas, J

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P.34 - Efficacy and safety of the recommended pegvaliase dosing regimen in adults with phenylketonuria in the phase 3 PRISM studies von Lindstrom, K, Sacharow, S, Northrup, H, Whitehall, KB, Rowell, R, Burton, B, Thomas, J

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FBN2 mutation associated with manifestations of Marfan syndrome and congenital contractural arachnodactyly von Gupta, P A, Wallis, D D, Chin, T O, Northrup, H, Tran-Fadulu, V T, Towbin, J A, Milewicz, D M

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Finding the genetic mechanisms of folate deficiency and neural tube defects—Leaving no stone unturned von Au, Kit Sing, Findley, Tina O., Northrup, Hope

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Benign multicystic peritoneal mesothelioma: cases reports in the family with diverticulosis and literature review von TANGJITGAMOL, S., ERLICHMAN, J., NORTHRUP, H., MALPICA, A., WANG, X., LEE, E., KAVANAGH, J.J.

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Mutational analysis of the tuberous sclerosis gene TSC2 in patients with pulmonary lymphangioleiomyomatosis von ASTRINIDIS, A, KHARE, L, CARSILLO, T, SMOLAREK, T, AU, K.-S, NORTHRUP, H, HENSKE, E. P

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Complete Inactivation of the TSC2 Gene Leads to Formation of Hamartomas von Au, Kit-Sing, Hebert, Adelaide A., Roach, E. Steve, Northrup, Hope

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Be Careful Around the Terabytes von Northrup, George H

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Epilepsy Risk Prediction Model for Patients With Tuberous Sclerosis Complex von Farach, Laura S., Richard, Melissa A., Lupo, Philip J., Sahin, Mustafa, Krueger, Darcy A., Wu, Joyce Y., Bebin, Elizabeth M., Au, Kit Sing, Northrup, Hope, Sahin, M., Krueger, D., Bebin, M., Wu, J.Y., Northrup, H., Warfield, S., Peters, J., Scherrer, B., Goyal, M., Filip-Dhima, R., Dies, K., Bruns, S., Hanson, E., Bing, N., Kent, B., O'Kelley, S., Williams, M.E., Pearson, D., Cutter, G., Roberds, S., Murray, D.S.

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Tuberous Sclerosis Complex Genotypes and Developmental Phenotype von Farach, Laura S., Pearson, Deborah A., Woodhouse, John P., Schraw, Jeremy M., Sahin, Mustafa, Krueger, Darcy A., Wu, Joyce Y., Bebin, Elizabeth M., Lupo, Philip J., Au, Kit Sing, Northrup, Hope, Sahin, M., Krueger, D., Bebin, M., Wu, J.Y., Northrup, H., Warfield, S., Peters, J., Scherrer, B., Goyal, M., Filip-Dhima, R., Dies, K., Bruns, S., Hanson, E., Bing, N., Kent, B., O'Kelley, S., Williams, M.E., Pearson, D., Cutter, G., Roberds, S., Murray, D.S.

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Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease von Kandt, R. S, Haines, J. L, Smith, M, Northrup, H, Gardner, R. J. M, Short, M. P, Dumars, K, Roach, E. S, Steingold, S, Wall, S, Blanton, S. H, Flodman, P, Kwiatkowski, D. J, Jewell, A, Weber, J. L, Roses, A. D, Pericak-Vance, M. A

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Brownian Dynamics of Cytochrome c and Cytochrome c Peroxidase Association von Northrup, Scott H., Boles, Jeffrey O., John C. L. Reynolds

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Genotype/phenotype correlation in 325 individuals referred for a diagnosis of tuberous sclerosis complex in the United States von Au, Kit Sing, Williams, Aimee T, Roach, E Steve, Batchelor, Lori, Sparagana, Steven P, Delgado, Mauricio R, Wheless, James W, Baumgartner, James E, Roa, Benjamin B, Wilson, Carolyn M, Smith-Knuppel, Teresa K, Cheung, Min-Yuen C, Whittemore, Vicky H, King, Terri M, Northrup, Hope

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Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation von Millen, Kathleen J, Grinberg, Inessa, Northrup, Hope, Ardinger, Holly, Prasad, Chitra, Dobyns, William B

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Examinations of Methylenetetrahydrofolate Reductase C677T and A1298C Mutations—and In Utero Viability von Volcik, K.A., Blanton, S.H., Northrup, H.

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