Estimating the power of a proposed linkage study for a complex genetic trait von PLOUGHMAN, L. M, BOEHNKE, M

Volltext

Randomized phase 2 study of carboplatin and bevacizumab in recurrent glioblastoma von Field, Kathryn M, Simes, John, Nowak, Anna K, Cher, Lawrence, Wheeler, Helen, Hovey, Elizabeth J, Brown, Christopher S B, Barnes, Elizabeth H, Sawkins, Kate, Livingstone, Ann, Freilich, Ron, Phal, Pramit M, Fitt, Greg, Rosenthal, Mark A

Volltext

Therapy with Efavirenz plus Indinavir in Patients with Extensive Prior Nucleoside Reverse-Transcriptase Inhibitor Experience: A Randomized, Double-Blind, Placebo-Controlled Trial von Haas, David W., Fessel, W. Jeffrey, Delapenha, Robert A., Kessler, Harold, Seekins, Daniel, Kaplan, Mark, Ruiz, Nancy M., Ploughman, Lynn M., Labriola, Dominic F., Manion, Douglas J.

Volltext

Major-locus contributions to variability of the craniofacial feature dystopia canthorum in Waardenburg syndrome von REYNOLDS, J. E, MARAZITA, M. L, MEYER, J. M, STEVENS, C. A, EAVES, L. J, ARNOS, K. S, PLOUGHMAN, L. M, MACLEAN, C, NANCE, W. E, DIEHL, S. R

Volltext

Biomarker Analyses in Phase 2 Single-Agent Trials of Dasatinib for Breast Cancer von Strauss, L., Sy, O., Fairchild, J., Fu, C., Rybicki, A., Yoganathan, S., Brickman, D., Harbison, C., Ploughman, L.

Volltext

Asp92Asn Polymorphism in the Myeloid IgA Fc Receptor Is Associated With Myocardial Infarction in Two Disparate Populations: CARE and WOSCOPS von Iakoubova, Olga A, Tong, Carmen H, Chokkalingam, Anand P, Rowland, Charles M, Kirchgessner, Todd G, Louie, Judy Z, Ploughman, Lynn M, Sabatine, Marc S, Campos, Hannia, Catanese, Joseph J, Leong, Diane U, Young, Bradford A, Lew, David, Tsuchihashi, Zenta, Luke, May M, Packard, Christopher J, Zerba, Kim E, Shaw, Peter M, Shepherd, James, Devlin, James J, Sacks, Frank M

Volltext

Dasatinib efficacy by dosing schedule across individual baseline BCR-ABL mutations in chronic phase chronic myelogenous leukemia (CML-CP) after imatinib failure von Hochhaus, A., Mueller, M., Cortes, J. E., Kim, D., Matlob, Y., Ploughman, L., Hughes, T.

Volltext

Evolution of the Role of Project Manager von Ploughman, Theodore L.

Volltext

Heterogeneity testing for Alzheimer's disease within and between data sets von Miller, L. L., Ploughman, L. M., Marazita, M. L.

Volltext

Genetic epidemiological studies of early-onset deafness in the U.S. school-age population von Marazita, Mary L., Ploughman, Lynn M., Rawlings, Brenda, Remington, Elizabeth, Arnos, Kathleen S., Nance, Walter E.

Volltext

A new test for linkage in the presence of locus heterogeneity von MacLean, C J, Ploughman, L M, Diehl, S R, Kendler, K S

Volltext

A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) gene von DIEHL, S. R, BOEHNKE, M, O'CONNELL, P, COLLINS, F. S, ERICKSON, R. P, PLOUGHMAN, L. M, SEILER, K. A, LIEBERMAN, J. L, CLARKE, H. B, BRUCE, M. A, SCHORRY, E. K, PERICAK-VANCE, M

Volltext

Severe hypoglycemia during pregnancy: Its frequency and predisposing factors in diabetic women von Rayburn, W., Piehl, E., Jacober, S., Schork, A., Ploughman, L.

Volltext

Prolonged mechanical ventilation and intracranial hemorrhage: impact on developmental progress through 18 months in infants weighing 1,200 grams or less at birth von BOZYNSKI, M. E. A, NELSON, M. N, MATALON, T. A. S, O'DONNELL, K. J, NAUGHTON, P. M, USHANALINI VASAN, MEIER, W. A, PLOUGHMAN, L

Volltext

Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8 von Diehl, S R, Boehnke, M, Collins, F S, Erickson, R P, Karolyi, I J, Ploughman, L M, Pericak-Vance, M A, Aylsworth, A S, Roses, A D

Volltext

Linkage analysis of von Recklinghausen neurofibromatosis to DNA markers on chromosome 17 von Diehl, S.R., Boehnke, M., Erickson, R.P., Baxter, A.B., Bruce, M.A., Lieberman, J.L., Platt, D.J., Ploughman, L.M., Seiler, K.A., Sweet, A.M., Collins, F.S.

Volltext

Prevalence of Spina Bifida at Birth - United States, 1983-1990: a Comparison of Two Surveillance Systems von Lary, Joseph M., Edmonds, Larry D.

Volltext

Testing for linkage under heterogeneity: a test versus C test von Faraway, J J

Volltext

A new test for linkage in the presence of locusheterogeneity von MACLEAN, C. J, PLOUGHMAN, L. M, DIEHL, S. R, KENDLER, K. S

Volltext

Analysis of Locus Heterogeneity in Waardenburg Syndrome Types 1 and 2 Using Highly Informative Microsatellite Markers von Reynolds, Jennifer E., Arnos, Kathleen S., Landa, Barbara, Stevens, Cathy A., Salbert, Bonnie A., Wright, Laura, Duke, Bettie, Hunt, Wanda, Marazita, Mary L., Ploughman, Lynn, MacLean, Charles, Nance, Walter E., Diehl, Scott R.

Volltext