Malignancy in Neurofibromatosis Type 1 von Korf, Bruce R.

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NF1 plexiform neurofibroma growth rate by volumetric MRI: relationship to age and body weight von Dombi, E, Solomon, J, Gillespie, A J, Fox, E, Balis, F M, Patronas, N, Korf, B R, Babovic-Vuksanovic, D, Packer, R J, Belasco, J, Goldman, S, Jakacki, R, Kieran, M, Steinberg, S M, Widemann, B C

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Genetic Heterogeneity of Saethre-Chotzen Syndrome, Due to TWIST and FGFR Mutations von Paznekas, William A., Cunningham, Michael L., Howard, Timothy D., Korf, Bruce R., Lipson, Mark H., Grix, Art W., Feingold, Murray, Goldberg, Rosalie, Borochowitz, Zvi, Aleck, Kirk, Mulliken, John, Yin, Mingfei, Jabs, Ethylin Wang

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DIAGNOSTIC OUTCOME IN CHILDREN WITH MULTIPLE CAFE-AU-LAIT SPOTS von KORF, BR

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NF1 Microdeletion Syndrome: Refined FISH Characterization of Sporadic and Familial Deletions with Locus-Specific Probes von Riva, Paola, Corrado, Lucia, Natacci, Federica, Castorina, Pierangela, Wu, Bai-Li, Schneider, Gretchen H., Clementi, Maurizio, Tenconi, Romano, Korf, Bruce R., Larizza, Lidia

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PTEN Mutation Spectrum and Genotype-Phenotype Correlations in Bannayan-Riley-Ruvalcaba Syndrome Suggest a Single Entity With Cowden Syndrome von Marsh, Debbie J., Kum, Jennifer B., Lunetta, Kathryn L., Bennett, Michael J., Gorlin, Robert J., Ahmed, S. Faisal, Bodurtha, Joann, Crowe, Carol, Curtis, Mary A., Dasouki, Majed, Dunn, Teresa, Feit, Howard, Geraghty, Michael T., Graham, John M., Hodgson, Shirley V., Hunter, Alasdair, Korf, Bruce R., Manchester, David, Miesfeldt, Susan, Murday, Victoria A., Nathanson, Katherine L., Parisi, Melissa, Pober, Barbara, Romano, Corrado, Tolmie, John L., Trembath, Richard, Winter, Robin M., Zackai, Elaine H., Zori, Roberto T., Weng, Liang-Ping, Dahia, Patricia L. M., Eng, Charis

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Deletion of the SLUG (SNAI2) gene results in human piebaldism von Sánchez-Martín, Manuel, Pérez-Losada, Jesús, Rodríguez-García, Arancha, González-Sánchez, Belén, Korf, Bruce R., Kuster, W., Moss, Celia, Spritz, Richard A., Sánchez-García, I.

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Somatic mosaicism for deletion of the entire NF1 gene identified by FISH von WU, B.-L, BOLES, R. G, YAARI, H, WEREMOWICZ, S, SCHNEIDER, G. H, KORF, B. R

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Phase 2 randomized, flexible crossover, double-blinded, placebo-controlled trial of the farnesyltransferase inhibitor tipifarnib in children and young adults with neurofibromatosis... von Widemann, Brigitte C, Dombi, Eva, Gillespie, Andrea, Wolters, Pamela L, Belasco, Jean, Goldman, Stewart, Korf, Bruce R, Solomon, Jeffrey, Martin, Staci, Salzer, Wanda, Fox, Elizabeth, Patronas, Nicholas, Kieran, Mark W, Perentesis, John P, Reddy, Alyssa, Wright, John J, Kim, AeRang, Steinberg, Seth M, Balis, Frank M

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The hereditary dystonias: An emerging story with a twist von Korf, Bruce R.

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Exploring concordance and discordance for return of incidental findings from clinical sequencing von Green, Robert C., Berg, Jonathan S., Berry, Gerard T., Biesecker, Leslie G., Dimmock, David P., Evans, James P., Grody, Wayne W., Hegde, Madhuri R., Kalia, Sarah, Korf, Bruce R., Krantz, Ian, McGuire, Amy L., Miller, David T., Murray, Michael F., Nussbaum, Robert L., Plon, Sharon E., Rehm, Heidi L., Jacob, Howard J.

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Diagnosis and management of neurofibromatosis type 1 von Korf, B R

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The effect of everolimus on renal angiomyolipoma in patients with tuberous sclerosis complex being treated for subependymal giant cell astrocytoma: subgroup results from the random... von Kingswood, J Chris, Jozwiak, Sergiusz, Belousova, Elena D, Frost, Michael D, Kuperman, Rachel A, Bebin, E Martina, Korf, Bruce R, Flamini, J Robert, Kohrman, Michael H, Sparagana, Steven P, Wu, Joyce Y, Brechenmacher, Thomas, Stein, Karen, Berkowitz, Noah, Bissler, John J, Franz, David N

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myc Gene amplification and expression in primary human neuroblastoma von SLAVC, I, ELLENBOGEN, R, WOO-HEE JUNG, VAWTER, G. F, KRETSCHMAR, C, GRIER, H, KORF, B. R

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Rib defects in patterns of multiple malformations: A retrospective review and phenotypic analysis of 47 cases von Wattanasirichaigoon, Duangrurdee, Prasad, Chitra, Schneider, Gretchen, Evans, Jane A., Korf, Bruce R.

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Stage III neuroblastoma over 1 year of age at diagnosis: improved survival with intensive multimodality therapy including multiple alkylating agents von WEST, D. C, SHAMBERGER, R. C, MACKLIS, R. M, KOZAKEWICH, H. P. W, WAYNE, A. S, KREISSMAN, S. G, KORF, B. R, LAVALLY, B, GRIER, H. E

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Genetic testing and medical practice von Korf, B R

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17q inversion involving the neurofibromatosis type one locus in a family with neurofibromatosis type one von Asamoah, Alexander, North, Kathryn, Doran, Steve, Wagstaff, Joseph, Ogle, Robert, Collins, Francis S., Korf, Bruce R.

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Townes-Brocks syndrome versus expanded spectrum hemifacial microsomia: Review of eight patients and further evidence of a “hot spot” for mutation in the SALL1 gene von Keegan, Catherine E., Mulliken, John B., Wu, Bai-Lin, Korf, Bruce R.

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Overview of Clinical Cytogenetics von Korf, Bruce R.

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