Rezultati - Robert J. Gorlin

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  1. 1
    Nevoid basal cell carcinoma (Gorlin) syndrome

    Nevoid basal cell carcinoma (Gorlin) syndrome od Robert J. Gorlin

    Izdano 2004
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  2. 2
    Nevoid Basal-Cell Carcinoma Syndrome

    Nevoid Basal-Cell Carcinoma Syndrome od Robert J. Gorlin

    Izdano 1987
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  3. 3
    Atlas of the Face in Genetic Disorders.

    Atlas of the Face in Genetic Disorders. od Richard M. Goodman, Robert J. Gorlin

    Izdano 1978
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  4. 4
    Primary malignant melanoma of the oral cavity. A review of 105 cases

    Primary malignant melanoma of the oral cavity. A review of 105 cases od A.P. Chaudhry, Anna Hampel, Robert J. Gorlin

    Izdano 1958
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  5. 5
    ODONTOGENIC TUMORS IN MAN AND ANIMALS: PATHOLOGIC CLASSIFICATION AND CLINICAL BEHAVIOR—A REVIEW*

    ODONTOGENIC TUMORS IN MAN AND ANIMALS: PATHOLOGIC CLASSIFICATION AND CLINICAL BEHAVIOR—A REVIEW* od Robert J. Gorlin, Lawrence H. Meskin, Robert S. Brodey

    Izdano 1963
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  6. 6
    Syndromes of the Head and Neck.

    Syndromes of the Head and Neck. od Robert J. Gorlin, Michael Cohen, Stefan L. Levin

    Izdano 1992
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  7. 7
    Odontogenic tumors.Classification, histopathology, and clinical behavior in man and domesticated animals

    Odontogenic tumors.Classification, histopathology, and clinical behavior in man and domesticated animals od Robert J. Gorlin, Anand P. Chaudhry, J. J. Pindborg

    Izdano 1961
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  8. 8
    Multiple mucosal neuromas, pheochromocytoma and medullary carcinoma of the thyroid—a syndrome

    Multiple mucosal neuromas, pheochromocytoma and medullary carcinoma of the thyroid—a syndrome od Robert J. Gorlin, Heddie O. Sedano, Robert A. Vickers, J Cervenka

    Izdano 1968
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  9. 9
    The multiple basal-cell nevi syndrome.An analysis of a syndrome consisting of multiple nevoid basal-cell carcinoma, jaw cysts, skeletal anomalies, medulloblastoma, and hyporesponsiveness to parathormone

    The multiple basal-cell nevi syndrome.An analysis of a syndrome consisting of multiple nevoid basal-cell carcinoma, jaw cysts, skeletal anomalies, medulloblastoma, and hyporesponsi... od Robert J. Gorlin, Robert A. Vickers, Elmer E. Kelln, John J. Williamson

    Izdano 1965
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  10. 10
    The calcifying odontogenic cyst.A new entity and possible analogue of the cutaneous calcifying epithelioma of malherbe

    The calcifying odontogenic cyst.A new entity and possible analogue of the cutaneous calcifying epithelioma of malherbe od Robert J. Gorlin, J. J. Pindborg, Robert S. Redman, John J. Williamson, Louis S. Hansen

    Izdano 1964
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  11. 11
    Mannosidosis: Clinical, Morphologic, Immunologic, and Biochemical Studies

    Mannosidosis: Clinical, Morphologic, Immunologic, and Biochemical Studies od Robert J. Desnick, Harvey L. Sharp, Gregory A. Grabowski, Richard D. Brunning, Paul G. Quie, Joo Ho Sung, Robert J. Gorlin, J. U. Ikonne

    Izdano 1976
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  12. 12
    In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome

    In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome od Laurence Faivre, Robert J. Gorlin, Mary K. Wirtz, Maurice Godfrey, Nathalie Dagoneau, J. R. Samples, Martine Le Merrer, Gwenaëlle Collod‐Béroud, Cathérine Boileau, Arnold Münnich, Valérie Cormier‐Daire

    Izdano 2003
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  13. 13
    Further delineation of the branchio‐oculo‐facial syndrome

    Further delineation of the branchio‐oculo‐facial syndrome od Angela E. Lin, Robert J. Gorlin, Iosif W. Lurie, Han G. Brunner, Ineke van der Burgt, I. V. Naumchik, Natalja V. Rumyantseva, S. Stengel‐Rutkowski, Kenneth N. Rosenbaum, Peter Meinecke, Dietmar Müller

    Izdano 1995
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  14. 14
    Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR

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

    Izdano 2004
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  15. 15
    Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans

    Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans od Stephen P. Robertson, Stephen R.F. Twigg, Andrew J. Sutherland‐Smith, Valérie Biancalana, Robert J. Gorlin, Denise Horn, Susan Kenwrick, Chong Ae Kim, Éva Morava, Ruth Newbury‐Ecob, Karen Helene Ørstavik, Oliver Quarrell, Charles E. Schwartz, Deborah Shears, Mohnish Suri, John Kendrick‐Jones, Andrew O.M. Wilkie

    Izdano 2003
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  16. 16
    Autosomal Dominant Craniometaphyseal Dysplasia Is Caused by Mutations in the Transmembrane Protein ANK

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

    Izdano 2001
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