Αποτελέσματα αναζήτησης - Robert J. Gorlin
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Nevoid basal cell carcinoma (Gorlin) syndrome από Robert J. Gorlin
Έκδοση 2004Revisão -
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Atlas of the Face in Genetic Disorders. από Richard M. Goodman, Robert J. Gorlin
Έκδοση 1978Artigo -
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Syndromes of the Head and Neck. από Robert J. Gorlin, Michael Cohen, Stefan L. Levin
Έκδοση 1992Artigo -
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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... από Robert J. Gorlin, Robert A. Vickers, Elmer E. Kelln, John J. Williamson
Έκδοση 1965Artigo -
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In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome από 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
Έκδοση 2003Artigo -
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Further delineation of the branchio‐oculo‐facial syndrome από 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
Έκδοση 1995Revisão -
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Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR από 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
Έκδοση 2004Artigo -
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Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans από 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
Έκδοση 2003Artigo -
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Autosomal Dominant Craniometaphyseal Dysplasia Is Caused by Mutations in the Transmembrane Protein ANK από 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
Έκδοση 2001Artigo
Εργαλεία αναζήτησης:
Σχετικά θέματα
Medicine
Pathology
Biology
Anatomy
Dentistry
Dermatology
Genetics
Basal cell
Gene
Locus (genetics)
Oral and maxillofacial pathology
Basal cell carcinoma
Carcinoma
Internal medicine
Nevoid basal-cell carcinoma syndrome
Oral and maxillofacial surgery
Oral medicine
Surgery
Acanthosis nigricans
Actin cytoskeleton
Alternative medicine
Archaeology
Astronomy
Atlas (anatomy)
Audiology
Brachydactyly
Calcification
Cancer research
Cell
Cell biology