Хайлтын үр дүнгүүд - Robert J. Gorlin
- 16-н 1 - 16 үр дүнгүүдийг харуулж байна
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Nevoid basal cell carcinoma (Gorlin) syndrome -н Robert J. Gorlin
Хэвлэсэн 2004Revisão -
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Atlas of the Face in Genetic Disorders. -н Richard M. Goodman, Robert J. Gorlin
Хэвлэсэн 1978Artigo -
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Syndromes of the Head and Neck. -н Robert J. Gorlin, Michael Cohen, Stefan L. Levin
Хэвлэсэн 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... -н Robert J. Gorlin, Robert A. Vickers, Elmer E. Kelln, John J. Williamson
Хэвлэсэн 1965Artigo -
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In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome -н 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
Хэвлэсэн 2003Artigo -
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Further delineation of the branchio‐oculo‐facial syndrome -н 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
Хэвлэсэн 1995Revisão -
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Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR -н 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
Хэвлэсэн 2004Artigo -
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Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans -н 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
Хэвлэсэн 2003Artigo -
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Autosomal Dominant Craniometaphyseal Dysplasia Is Caused by Mutations in the Transmembrane Protein ANK -н 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
Хэвлэсэн 2001Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
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