Cardiac involvement in myotonic dystrophy: a nationwide cohort study von Lund, Marie, Diaz, Lars Jorge, Ranthe, Mattis Flyvholm, Petri, Helle, Duno, Morten, Juncker, Inger, Eiberg, Hans, Vissing, John, Bundgaard, Henning, Wohlfahrt, Jan, Melbye, Mads

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Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation von HAUBEK, DORTE, GJØRUP, HANS, JENSEN, LILLIAN G., JUNCKER, INGER, NYEGAARD, METTE, BØRGLUM, ANDERS D., POULSEN, SVEN, HERTZ, JENS M.

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Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation: FAM83H-associated hypocalcified AI von HAUBEK, DORTE, GJØRUP, HANS, JENSEN, LILLIAN G., JUNCKER, INGER, NYEGAARD, METTE, BØRGLUM, ANDERS D., POULSEN, SVEN, HERTZ, JENS M.

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Alport syndrome caused by inversion of a 21 Mb fragment of the long arm of the X-chromosome comprising exon 9 through 51 of the COL4A5 gene von HERTZ, Jens Michael, PERSSON, Uif, JUNCKER, Inger, SEGELMARK, Marten

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Patients with Goodpasture's disease have two normal COL4A3 alleles encoding the NC1 domain of the type IV collagen α3 chain von Persson, Ulf, Hertz, Jens Michael, Carlsson, Malin, Hellmark, Thomas, Juncker, Inger, Wieslander, Jörgen, Segelmark, Mårten

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Patients with Goodpasture's disease have two normal COL4A3 alleles encoding the NC1 domain of the type IV collagen alpha 3 chain von Persson, Ulf, Hertz, Jens Michael, Carlsson, Malin, Hellmark, Thomas, Juncker, Inger, Wieslander, Jörgen, Segelmark, Mårten

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Detection of mutations in the COL4A5 gene by SSCP in X‐linked Alport syndrome von Hertz, Jens Michael, Juncker, Inger, Persson, Ulf, Matthijs, Gert, Schmidtke, Jörg, Petersen, Michael B., Kjeldsen, Margrethe, Gregersen, Niels

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Patients with Goodpasture's disease have two normal COL4A3 alleles encoding the NC1 domain of the type IV collagen  3 chain von Persson, U., Hertz, J. M., Carlsson, M., Hellmark, T., Juncker, I., Wieslander, J., Segelmark, M.

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Family studies of complement C4 and HLA in man von Bruun-Petersen, G, Lamm, L U, Sørensen, I J, Buskjaer, L, Mortensen, J P

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A novel missense mutation (402C → T) in exon 1 in the EDA gene in a family with X-linked hypohidrotic ectodermal dysplasia von Hertz, Jens Michael, Hansen, Karen Nørgaard, Juncker, Inger, Kjeldsen, Margrethe, Gregersen, Niels

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Genetic studies of complement C4 in man von Petersen, G B, Sørensen, I J, Buskjaer, L, Lamm, L U

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