Результати пошуку - B. Castle
- Показ 1 - 14 результатів із 14
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Evaluation of genotype-phenotype correlations in neurofibromatosis type 1 за авторством B. Castle
Опубліковано 2003Carta -
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SEQUENTIAL MECHANISMS IN THE ENHANCED ABSORPTION OF VITAMIN B12 BY INTRINSIC FACTOR IN THE RAT* за авторством Bernard A. Cooper, William B. Castle
Опубліковано 1960Artigo -
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IN VITRO ASSAY FOR HUMAN INTRINSIC FACTOR* за авторством Louis W. Sullivan, Victor Herbert, William B. Castle
Опубліковано 1963Artigo -
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STUDIES ON THE DESTRUCTION OF RED BLOOD CELLS. XII. FACTORS INFLUENCING THE ROLE OF S HEMOGLOBIN IN THE PATHOLOGIC PHYSIOLOGY OF SICKLE CELL ANEMIA AND RELATED DISORDERS 1 за авторством Mortimer S. Greenberg, Edward H. Kass, William B. Castle
Опубліковано 1957Artigo -
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STUDIES ON THE DESTRUCTION OF RED BLOOD CELLS за авторством SHU CHU SHEN, Eleanor Fleming, W. B. Castle
Опубліковано 1949Artigo -
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QUANTITATIVE ASPECTS OF IRON DEFICIENCY IN HYPOCHROMIC ANEMIA за авторством Clark W. Heath, Maurice B. Strauss, William B. Castle
Опубліковано 1932Artigo -
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Red Cell Filtration and the Pathogenesis of Certain Hemolytic Anemias за авторством James H. Jandl, Richard L. Simmons, William B. Castle
Опубліковано 1961Artigo -
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STUDIES ON THE DESTRUCTION OF RED BLOOD CELLS. IV за авторством Thomas Hale Ham, SHU CHU SHEN, Eleanor Fleming, W. B. Castle
Опубліковано 1948Artigo -
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Phenotype and genotype in 17 patients with Goltz-Gorlin syndrome за авторством Saskia M. Maas, Maria Lombardi, A. J. van Essen, Emma Wakeling, B. Castle, I. Karen Temple, Vibhore Kumar, Karin Writzl, Raoul C. M. Hennekam
Опубліковано 2009Artigo -
14
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome за авторством Bregje W.M. van Bon, Heather C. Mefford, Björn Menten, David A. Koolen, Andrew J. Sharp, Willy M. Nillesen, Jeffrey W. Innis, Thomy de Ravel, Catherine L. Mercer, Marco Fichera, Helen Stewart, Louise Connell, Katrin Õunap, Katherine Lachlan, B. Castle, Nathalie Van der Aa, Conny van Ravenswaaij, Marcelo A. Nóbrega, Clara Serra‐Juhé, Ingrid Simonic, Nicole de Leeuw, Rolph Pfundt, Ernie M.H.F. Bongers, Carl Baker, P Finnemore, Shuwen Huang, V. Maloney, John A. Crolla, M van Kalmthout, Maurizio Elia, Geert Vandeweyer, J. P. Fryns, Sandra Janssens, Nicola Foulds, S Reitano, Kath Smith, Sven Parkel, Bart Loeys, C. Geoffrey Woods, Anna Oostra, Frank Speleman, Alexandre C. Pereira, Ants Kurg, Lionel Willatt, Samantha J.L. Knight, Joris Vermeesch, Corrado Romano, John Barber, Geert Mortier, Luis Alberto Pérez‐Jurado, R. Frank Kooy, Han G. Brunner, Evan E. Eichler, Tjitske Kleefstra, Bert B.A. de Vries
Опубліковано 2009Artigo
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Пов'язані теми
Biology
Medicine
Chemistry
Immunology
Internal medicine
Biochemistry
Genetics
Biophysics
Gene
Phenotype
Anemia
Cell biology
Fetus
Hemolytic anemia
Intrinsic factor
Mutation
Physics
Physiology
Pregnancy
Red Cell
Red blood cell
Absorption (acoustics)
Antibody
Camptodactyly
Clinical significance
Computational biology
Congenital disease
Copy-number variation
Cyanocobalamin
Dehydrogenase