In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome von Faivre, L, Gorlin, R J, Wirtz, M K, Godfrey, M, Dagoneau, N, Samples, J R, Le Merrer, M, Collod-Beroud, G, Boileau, C, Munnich, A, Cormier-Daire, V

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Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency disease von Diaz, George A, Hernandez, Paolo A, Gorlin, Robert J, Lukens, John N, Taniuchi, Shoichiro, Bohinjec, Jo e, Francois, Fleur, Klotman, Mary E

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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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Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR von Black, Graeme C M, Ng, David, Thakker, Nalin, Corcoran, Connie M, Donnai, Dian, Perveen, Rahat, Schneider, Adele, Hadley, Donald W, Tifft, Cynthia, Zhang, Liqun, Wilkie, Andrew O M, van der Smagt, Jasper J, Gorlin, Robert J, Burgess, Shawn M, Bardwell, Vivian J, Biesecker, Leslie G

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Germline Mutations in the PTEN/MMAC1 Gene in Patients With Cowden Disease von Nelen, Marcel R., van Staveren, Wilma C. G., Peeters, Els A. J., Ben Hassel, Mohammed, Gorlin, Robert J., Hamm, Henning, Lindboe, Christian F., Fryns, Jean-Pierre, Sijmons, Rolf H., Woods, D. Geoffrey, Mariman, Edwin C. M., Padberg, George W., Kremer, Hannie

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A two-hit model for developmental defects in Gorlin syndrome von Levanat, Sonja, Gorlin, Robert J, Fallet, Shari, Johnson, Dennis R, Fantasia, John E, Bale, Alien E

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Germline mutations in PTEN are present in Bannayan-Zonana syndrome von Marsh, Debbie J, Dahia, Patricia L. M, Zheng, Zimu, Liaw, Danny, Parsons, Ramon, Gorlin, Robert J, Eng, Charis

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Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromes von Zhou, Xiao-Ping, Hampel, Heather, Thiele, Hannelore, Gorlin, Robert J, Hennekam, Raoul CM, Parisi, Melissa, Winter, Robin M, Eng, Charis

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Autosomal Dominant Craniometaphyseal Dysplasia Is Caused by Mutations in the Transmembrane Protein ANK von Reichenberger, Ernst, Tiziani, Valdenize, Watanabe, Shoji, Park, Lucy, Ueki, Yasuyoshi, Santanna, Carla, Baur, Scott T., Shiang, Rita, Grange, Dorothy K., Beighton, Peter, Gardner, Jessica, Hamersma, Herman, Sellars, Sean, Ramesar, Rajkumar, Lidral, Andrew C., Sommer, Annmarie, Raposo do Amaral, Cassio M., Gorlin, Robert J., Mulliken, John B., Olsen, Bjorn R.

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Clinical homogeneity and genetic heterogeneity in Weill-Marchesani syndrome von Faivre, Laurence, Dollfus, Hélène, Lyonnet, Stanislas, Alembik, Yves, Mégarbané, André, Samples, John, Gorlin, Robert J., Alswaid, Abdulrahman, Feingold, Josué, Le Merrer, Martine, Munnich, Arnold, Cormier-Daire, Valérie

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Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts von Barrow, L L, van Bokhoven, H, Daack-Hirsch, S, Andersen, T, van Beersum, S E C, Gorlin, R, Murray, J C

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Of palms, soles, and gums von GORLIN, ROBERT J

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Nevoid basal cell carcinoma (Gorlin) syndrome von Gorlin, Robert J.

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Effects of long-term, moderate-intensity oral anticoagulation in addition to aspirin in unstable angina von The Organization to Assess Strategies for Ischemic Syndromes (OASIS) Investigators

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Nevoid basal-cell carcinoma syndrome von Gorlin, R J

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Fibroblast growth factors, their receptors and receptor disorders von Gorlin, R.J.

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Melanotic neuroectodermal tumor of infancy. A reexamination of a histogenetic problem based on immunohistochemical, flow cytometric, and ultrastructural study of 10 cases von Pettinato, G, Manivel, J C, d'Amore, E S, Jaszcz, W, Gorlin, R J

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THE MARITIME OPERATIONAL THREAT RESPONSE PLAN: A MODEL FOR INTERAGENCY COOPERATION von Gorlin, Lee R

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Craniotubular bone disorders von GORLIN, R. J

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Syndromes, Syndromes, and More Syndromes von Gorlin, Robert J.

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