A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental disease von Ku, C S, Polychronakos, C, Tan, E K, Naidoo, N, Pawitan, Y, Roukos, D H, Mort, M, Cooper, D N

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Galectins. Structure and function of a large family of animal lectins von Barondes, S H, Cooper, D N, Gitt, M A, Leffler, H

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Sequence and specificity of a soluble lactose-binding lectin from Xenopus laevis skin von MARSCHAL, P, HERRMANN, J, LEFFLER, H, BARONDES, S. H, COOPER, D. N. W

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Utilization of a cryptic noncanonical donor splice site in the KRT14 gene causes a mild form of epidermolysis bullosa simplex: KRT14 gene and EBS von Han, S., Cooper, D.N., Bowden, P.E.

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Complement component C7 deficiency in four Irish families: The characterisation of a large genomic deletion within the C7 gene von Thomas, A.D., Roberts, A.G., Chuzhanova, N., Cooper, D.N., Feighery, C., Connaughton, J., Morgan, B.P., Orren, A.

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Comparative analysis of copy number variation in primate genomes von Kehrer-Sawatzki, H., Cooper, D.N.

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Utilization of a cryptic noncanonical donor splice site in the KRT14 gene causes a mild form of epidermolysis bullosa simplex von Han, S., Cooper, D.N., Bowden, P.E.

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Evidence for Export of a Muscle Lectin from Cytosol to Extracellular Matrix and for a Novel Secretory Mechanism von Douglas N. W. Cooper, Barondes, Samuel H.

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Chromosomal speciation of humans and chimpanzees revisited: studies of DNA divergence within inverted regions von Szamalek, J.M., Cooper, D.N., Hoegel, J., Hameister, H., Kehrer-Sawatzki, H.

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Rat olfactory neurons can utilize the endogenous lectin, L-14, in a novel adhesion mechanism von MAHANTHAPPA, N. K, COOPER, D. N. W, BARONDES, S. H, SCHWARTING, G. A

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Flow of cerebral interstitial fluid as indicated by the removal of extracellular markers from rat caudate nucleus von Cserr, Helen F., Cooper, D.N., Milhorat, T.H.

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Gross Deletions and Translocations in Human Genetic Disease von Abeysinghe, S.S., Chuzhanova, N., Cooper, D.N.

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Verifying nomenclature of DNA variants in submitted manuscripts: guidance for journals von Higgins, J., Dalgleish, R., Dunnen, J.T. den, Barsh, G., Freeman, P.J., Cooper, D.N., Cullinan, S., Davies, K.E., Dorkins, H., Gong, L., Imoto, I., Klein, T.E., Korf, B., Misra, A., Paalman, M.H., Ratzel, S., Reichardt, J.K.V., Rehm, H.L., Tokunaga, K., Weck, K.E., Cutting, G.R.

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Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition von Tuddenham, E.G.D., Schwaab, R., Seehafer, J., Millar, D.S., Gitschier, J., Higuchi, M., Bidichandani, S., Connor, J.M., Hoyer, L.W., Yoshioka, A., Peake, I.R., Olek, K., Kazazian, H.H., Lavergne, J.-M., Giannelli, F., Antonarakis, S.E., Cooper, D.N.

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Haemophilia A: database of ncleotide substituttions, deletions, insertions and rearrangements of the factor VIII gene von Tuddenham, E.G.D., Cooper, D.N., Gitschier, J., Higuchi, M., Hoyer, L.W., Yoshioka, A., Peake, I.R., Schwaab, R., Olek, K., Kazazian, H.H., Lavergne, J.M., Giannelli, F., Antonarakis, S.E.

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Diagnosis of human genetic disease using recombinant DNA : fourth edition von COOPER, D. N, SCHMIDTKE, J

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Molecular analysis of the genotype-phenotype relationship in factor X deficiency von Millar, D.S., Elliston, L., Deex, P., Krawczak, M., Wacey, A.I., Reynaud, J., Nieuwenhuis, H.K., Bolton-Maggs, P., Mannucci, P.M., Reverter, J.C., Cachia, P., Pasi, K.J., Layton, D.M., Cooper, D.N.

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Late-onset homozygous protein C deficiency von Grundy, C.B, Melissari, E, Lindo, V, Scully, M.F, Kakkar, V.V, Cooper, D.N

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Diagnosis of genetic disease using recombinant DNA. Third edition von COOPER, D. N, SCHMIDTKE, J

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HUMAN GENE CLONING AND DISEASE ANALYSIS von Cooper, D.N., Schmidtke, J.

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