Genetic and Physical Mapping of the Locus for Autosomal Dominant Renal Fanconi Syndrome, on Chromosome 15q15.3 von Lichter-Konecki, U., Broman, K.W., Blau, E.B., Konecki, D.S.

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The primary structure of human chromogranin A and pancreastatin von Konecki, D S, Benedum, U M, Gerdes, H H, Huttner, W B

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Molecular Basis of Phenotypic Heterogeneity in Phenylketonuria von Okano, Yoshiyuki, Eisensmith, Randy C, Güttler, Flemming, Lichter-Konecki, Uta, Konecki, David S, Trefz, Friedrich K, Dasovich, Mary, Wang, Tao, Henriksen, Karen, Lou, Hans, Woo, Savio L.C

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Structure, Expression, and Mutation of the Hypoxanthine Phosphoribosyltransferase Gene von Melton, David W., Konecki, David S., Brennand, John, Caskey, C. Thomas

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The primary structure of bovine chromogranin A: a representative of a class of acidic secretory proteins common to a variety of peptidergic cells von Benedum, U.M., Baeuerle, P.A., Konecki, D.S., Frank, R., Powell, J., Mallet, J., Huttner, W.B.

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The primary structure of human secretogranin I (chromogranin B): comparison with chromogranin A reveals homologous terminal domains and a large intervening variable region von Benedum, U. M., Lamouroux, A., Konecki, D. S., Rosa, P., Hille, A., Baeuerle, P. A., Frank, R., Lottspeich, F., Mallet, J., Huttner, W. B.

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Expression patterns of murine lysosome-associated membrane protein 2 (Lamp-2) transcripts during morphogenesis von Lichter-Konecki, Uta, Moter, Sabine E., Krawisz, Bruce R., Schlotter, Magdalena, Hipke, Christine, Konecki, David S.

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Alternative splicing in the fragile X gene FMR1 von Verkerk, Annemieke J.M.H., de Graaff, Esther, De Boulle, Kristel, Eichler, Evan E., Konecki, David S., Reyniers, Edwin, Manca, Antonella, Poustka, Annemarie, Willems, Patrick J., Nelson, David L., Oostra, Ben A.

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Hypoxanthine-guanine phosphoribosyltransferase genes of mouse and Chinese hamster: construction and sequence analysis of cDNA recombinants von Konecki, David S., Brennand, John, Fuscoe, James C., Caskey, C.Thomas, Chinault, A.Craig

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The phenylketonuria locus : current knowledge about alleles and mutations of the phenylalanine hydroxylase gene in various populations von KONECKI, D. S, LICHTER-KONECKI, U

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Construction of a transcription map of a 300 kb region around the human G6PD locus by direct cDNA selection von SEDLACEK, Z, KORN, B, KONECKI, D. S, SIEBENHAAR, R, COY, J. F, KIOSCHIS, P, POUSTKA, A

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Phenylalanine hydroxylase genotypes, predicted residual enzyme activity and phenotypic parameters of diagnosis and treatment of phenylketonuria von Burgard, P, Rupp, A, Konecki, D S, Trefz, F K, Schmidt, H, Lichter-Konecki, U

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Structural characterization of the 5' regions of the human phenylalanine hydroxylase gene von Konecki, David S, Wang, Yibin, Trefz, Friedrich K, Lichter-Konecki, Uta, Woo, Savio L. C

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Human Phenylalanine Hydroxylase Gene Expression in Kidney and Other Nonhepatic Tissues von Lichter-Konecki, Uta, Hipke, Christine M., Konecki, David S.

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TurboPrep II: An Inexpensive, High-Throughput Plasmid Template Preparation Protocol von Konecki, David S, Phillips, Jennifer J

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An Alternatively Spliced Form of the Human Lysosome-Associated Membrane Protein-2 Gene Is Expressed in a Tissue-Specific Manner von Konecki, D.S., Foetisch, K., Zimmer, K.P., Schlotter, M., Konecki, U.L.

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DNA sequence polymorphisms in exonic and intronic regions of the human phenylalanine hydroxylase gene aid in the identification of alleles von LICHTER-KONECKI, U, SCHLOTTER, M, KONECKI, D. S

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Alternative splicing in the fragile X gene FMR1 von Verkerk, A.J.M.H., de Graaff, E., De Boulle, K., Eichler, E.E., Konecki, D.S., Reyniers, E., Manca, A., Poustka, A., Willems, P.J., Nelson, D.L., Oostra, B.A.

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Evolutionary conservation and genomic organization of XAP-4, an Xq28 located gene coding for a human rab GDP-dissociation inhibitor (GDI) von Sedlacek, Z, Konecki, D S, Korn, B, Klauck, S M, Poustka, A

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Geographical distribution of the P281L mutation at the phenylalanine hydroxylase locus: possible origin in southeastern Europe von Barić, I., Mardešić, D., Sarnavøka, V., Lichter‐Konecki, U., Konecki, D. S., Trefz, F. K.

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