Mapping of novel regions of DNA gain and loss by comparative genomic hybridization in esophageal carcinoma in the Black and colored populations of South Africa von PLESSIS, L. D, DIETZSCH, E, SPELEMAN, F, VAN GELE, M, VAN ROY, N, VAN HELDEN, P, PARKER, M. I, MUGWANYA, D. K, DE GROOT, M, MARX, M. P, KOTZE, M. J

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High prevalence of the CYS282TYR HFE mutation facilitates an improved diagnostic service for hereditary haemochromatosis in South Africa von DE VILLIERS, J. N. P, HILLERMAN, R, DE JONG, G, LANGENHOVEN, E, ROSSOUW, H, MARX, M. P, KOTZE, M. J

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Inherited colon cancers von Goldberg, P A, Madden, M V, Harocopos, C, Grobbelaar, J J, Kotze, M J, Marx, M P, de Jong, G, Ramesar, R

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The identification of two low-density lipoprotein receptor gene mutations in South African familial hypercholesterolaemia von KOTZE, M. J, LANGENHOVEN, E, WARNICH, L, DU PLESSIS, L, MARX, M. P, OOSTHUIZEN, C. J. J, RETIEF, A. E

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Eyelid Mass Secondary to T-Cell Lymphoma in a Child: A Rare Presentation and Literature Review von Ram, Radha, MD, Marolf, Marissa D., BS, Marx, Douglas P., MD, Braverman, Richard M., MD, Firan, Mihail, MD, Herce, Honey H., MD

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Comprehensive TP53-Denaturing Gradient Gel Electrophoresis Mutation Detection Assay Also Applicable to Archival Paraffin-Embedded Tissue von Hayes, Vanessa M, Bleeker, Wim, Verlind, Edwin, Timmer, Tineke, Karrenbeld, Arend, Plukker, John T, Marx, Munro P, Hofstra, Robert M. W, Buys, Charles H. C. M

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Molecular characterisation of a low-frequency mutation in exon 8 of the human low-density lipoprotein receptor gene von Kotze, M J, Langenhoven, E, Warnich, L, Marx, M P, Retief, A E

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The psychophysiological correlates of risk recognition among victims and non-victims of sexual assault von Soler-Baillo, Jose M., Marx, Brian P., Sloan, Denise M.

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Two novel and two known low-density lipoprotein receptor gene mutations in German patients with familial hypercholesterolemia von Thiart, Rochelle, Loubser, Odell, de Villiers, J. Nico P., Marx, Munro P., Zaire, Reinhardt, Raal, Frederick J., Kotze, Maritha J.

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Combined (team) approach to hemangioma management: arteriography with superselective embolization plus YAG laser/sapphire-tip resection von Apfelberg, D B, Lane, B, Marx, M P

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Prenatal diagnosis of Fanconi's anemia von Marx, M P, Dawson, B, Heyns, A D

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A nonsense mutation (Arg-196-Term) in exon 6 of the human TP53 gene identified in small cell lung carcinoma von Hayes, Vanessa M., Oosthuizen, C.J.Joubert, Kotze, Maritha J., Marx, Munro P., Buys, Charles H.C.M.

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Fanconi's anemia: A cytogenetic study on lymphocyte and bone marrow cultures utilizing 1,2:3,4-diepoxybutane von Marx, M.P., Smith, S., Heyns, A.du P., van Tonder, I.Z.

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Simultaneous occurrence of heritable t(3;7) and t(14;21) in two sibs von Kruger, A J, Jansen, S, Marx, M P, Coetzee, D J, Cilliers, A E, Human, S, Spies, I Z, Roux, F

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A confirmed prenatal diagnosis of a female fetus with the fragile X chromosome von Venter, Philippus A., Coetzee, Dennis J., Badenhorst, Anelie, Marx, Munro P., Hof, Johann Op't, Behari, Dhana, Wilmot, Jenny, Battson, Shareen A.

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Combined (team) approach to hemangioma management : arteriography with superselective embolilization plus YAG laser/sapphire-tip resection von APFELBERG, D. B, LANE, B, MARX, M. P

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Simultaneous occurence of heritable t(3; 7) and t(14; 21) in two sibs von KRUGER, A. J, JANSEN, S, MARX, M. P, COETZEE, D. J, CILLIERS, A. E, HUMAN, S, SPIES, I. Z, ROUX, F

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Prenatal diagnosis of Fanconi's anemia von Marx, M P, Dawson, B, Heyns, A D

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The Clinician-Administered PTSD Scale for DSM-5 (CAPS-5): Development and Initial Psychometric Evaluation in Military Veterans von Weathers, Frank W., Bovin, Michelle J., Lee, Daniel J., Sloan, Denise M., Schnurr, Paula P., Kaloupek, Danny G., Keane, Terence M., Marx, Brian P.

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Psychometric Properties of the PTSD Checklist for Diagnostic and Statistical Manual of Mental Disorders-Fifth Edition (PCL-5) in Veterans von Bovin, Michelle J., Marx, Brian P., Weathers, Frank W., Gallagher, Matthew W., Rodriguez, Paola, Schnurr, Paula P., Keane, Terence M.

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