Inversion of the IDS gene resulting from recombination with IDS-related sequences in a common cause of the Hunter syndrome von Bondeson, Maire-Louise, Dahl, Niklas, Malmgren, Helena, Kleijer, Wim J., Tönnesen, Tönne, Carlberg, Britt-Marie, Pettersson, Ulf

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Double-Strand Breaks May Initiate the Inversion Mutation Causing the Hunter Syndrome von Lagerstedt, Kristina, Karsten, Stanislav L., Carlberg, Britt-Marie, Kleijer, Wim J., Tönnesen, Tönne, Pettersson, Ulf, Bondeson, Marie-Louise

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Menkes Disease: An X-Linked Neurological Disorder of the Copper Metabolism von Horn, Nina, Tønnesen, Tønne, Türner, Zeynep

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Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein von Chelly, Jamel, Tümer, Zeynep, Tønnesen, Tønne, Petterson, Anne, Ishikawa-Brush, Yumiko, Tommerup, Niels, Horn, Nina, Monaco, Anthony P

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Identification of point mutations in 41 unrelated patients affected with Menkes disease von TÜMER, Z, LUND, C, TOLSHAVE, J, VURAL, B, TØNNESEN, T, HORN, N

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Early copper-histidine treatment for Menkes disease von Tümer, Zeynep, Horn, Nina, Tønnesen, Tønne, Christodoulou, John, Clarke, Joe T.R, Sarkar, Bibudhendra

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Characterization of the exon structure of the Menkes disease gene using vectorette PCR von Tümer, Z., Vural, B., Tønnesen, T., Chelly, J., Monaco, A.P., Horn, N.

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Characterization of a 1.0 Mb YAC contig spannning two chromosome breakpoints related to Menkes disease von Tümer, Zeynep, Chelly, Jamel, Tommerup, Niels, Ishikawa-Brush, Yumiko, Tønnesen, Tønne, Monaco, Anthony P., Horn, Nina

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Mutations in the arylsulfatase A pseudodeficiency allele causing metachromatic leukodystrophy von GIESELMAN, V, FLUHARTY, A. L, TØNNESEN, T, VON FIGURA, K

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First trimester prenatal diagnosis of Menkes disease by DNA analysis von Tümer, Z, Tønnesen, T, Böhmann, J, Marg, W, Horn, N

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Studies on the Amount and Location of the tRNA and 5‐S rRNA Genes in Tetrahymena pyriformis GL von TØNNESEN, Tønne, ENGBERG, Jan, LEICK, Vagn

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Genotype-phenotype relationship in various degrees of arylsulfatase A deficiency von KAPPLER, J, LEINEKUGEL, P, CONZELMANN, E, KLEIJER, W. J, KOHLSCHÜTTER, A, TØNNESEN, T, ROCHEL, M, FREYCON, F, PROPPING, P

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Evidence for existence of messenger ribonucleoprotein complexes in Tetrahymena pyriformis von Tonnesen, T

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Comparison of trace element distributions in occipital horn syndrome and menkes disease with normal subjects by neutron activation analysis von Heydorn, Kaj, Damsgaard, Else, Horn, Nina, Tønnesen, Tønne, Mussalo‐Rauhamaa, Helena, Kaitila, Ilkka

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Diagnosis of Hunter's syndrome carriers; radioactive sulphate incorporation into fibroblasts in the presence or fructose 1-phosphate von Tønnesen, T, Lykkelund, C, Güttler, F

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Isolation of two small molecular weight RNA components by MAK column chromatography von Frederiksen, Sune, Tønnesen, Tønne, Hellung-Larsen, Per

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Trichothiodystrophy, mental retardation, short stature, ataxia, and gonadal dysfunction in three Moroccan siblings von Przedborski, Serge, Ferster, Alina, Goldman, Sylvie, Wolter, Renée, Song, Micheline, Tonnesen, Tonne, Pollitt, Rodney J., Vamos, Esther

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