Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2 von KAMSTEEG, Erik-Jan, KRESS, Wolfram, CATALLI, Claudio, HERTZ, Jens M, WITSCH-BAUMGARTNER, Martina, BUCKLEY, Michael F, ENGELEN, Baziel Gm Van, SCHWARTZ, Marianne, SCHEFFER, Hans

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Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness von Davidson, Alice E, Cheong, Sek-Shir, Hysi, Pirro G, Venturini, Cristina, Plagnol, Vincent, Ruddle, Jonathan B, Ali, Hala, Carnt, Nicole, Gardner, Jessica C, Hassan, Hala, Gade, Else, Kearns, Lisa, Jelsig, Anne Marie, Restori, Marie, Webb, Tom R, Laws, David, Cosgrove, Michael, Hertz, Jens M, Russell-Eggitt, Isabelle, Pilz, Daniela T, Hammond, Christopher J, Tuft, Stephen J, Hardcastle, Alison J

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Myoblasts generated by lentiviral mediated MyoD transduction of myotonic dystrophy type 1 (DM1) fibroblasts can be used for assays of therapeutic molecules von Larsen, Jan, Pettersson, Olof J, Jakobsen, Maria, Thomsen, Rune, Pedersen, Christina B, Hertz, Jens M, Gregersen, Niels, Corydon, Thomas J, Jensen, Thomas G

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Association between periacetabular osteotomy and hip dysplasia among relatives: a cross-sectional study von Simonsen, Pernille O, Hertz, Jens M, Søballe, Kjeld, Mechlenburg, Inger

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Chromosomal Aberrations in Monozygotic and Dizygotic Twins Versus Singletons in Denmark During 1968–2009 von Kroeldrup, Lone, Larsen, Lisbeth A., Fagerberg, Christina, Hertz, Jens M., Christensen, Kaare

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Eating behavior, prenatal and postnatal growth in Angelman syndrome von Mertz, Line G.B., Christensen, Rikke, Vogel, Ida, Hertz, Jens M., Østergaard, John R.

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The Association between Gender and Familial Prevalence of Hip Dysplasia in Danish Patients von Jashi, Rima El, Gustafson, Maria B., Jakobsen, Mette B., Lautrup, Charlotte, Hertz, Jens M., Søballe, Kjeld, Mechlenburg, Inger

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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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A novel missense mutation (G43S) in the switch I region of Rab27A causing Griscelli syndrome von Westbroek, Wendy, Tuchman, Maya, Tinloy, Bradford, De Wever, Olivier, Vilboux, Thierry, Hertz, Jens M., Hasle, Henrik, Heilmann, Carsten, Helip-Wooley, Amanda, Kleta, Robert, Gahl, William A.

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Detailed investigations of proximal tubular function in Imerslund-Gräsbeck syndrome von Storm, Tina, Zeitz, Christina, Cases, Olivier, Amsellem, Sabine, Verroust, Pierre J, Madsen, Mette, Benoist, Jean-François, Passemard, Sandrine, Lebon, Sophie, Jønsson, Iben Møller, Emma, Francesco, Koldsø, Heidi, Hertz, Jens Michael, Nielsen, Rikke, Christensen, Erik I, Kozyraki, Renata

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Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism von Karadima, Georgia, Bugge, Merete, Nicolaidis, Peter, Vassilopoulos, Dimitris, Avramopoulos, Dimitris, Grigoriadou, Maria, Albrecht, Beate, Passarge, Eberhard, Annerén, Göran, Blennow, Elisabeth, Clausen, Niels, Galla-Voumvouraki, Angeliki, Tsezou, Aspasia, Kitsiou-Tzeli, Sofia, Hahnemann, Johanne M, Hertz, Jens M, Houge, Gunnar, Kuklík, Miloslav, Macek, Milan, Lacombe, Didier, Miller, Konstantin, Moncla, Anne, Pajares, I López, Patsalis, Philippos C, Prieur, Marguerite, Vekemans, Michel, von Beust, Gabriela, Brøndum-Nielsen, Karen, Petersen, Michael B

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Cathepsin K gene mutations and 1q21 haplotypes in at patients with pycnodysostosis in an outbred population von Haagerup, A, Hertz, J M, Christensen, M F, Binderup, H, Kruse, T A

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Mutation pattern in the Bruton's tyrosine kinase gene in 26 unrelated patients with X-linked agammaglobulinemia von Vorřechovský, Igor, Luo, Liping, Hertz, Jens M., Frøland, Stig S., Klemola, Timo, Fiorini, Maurilia, Quinti, Isabella, Paganelli, Roberto, Ozsahin, Hulya, Hammarström, Lennart, Webster, A. David B., Smith, C. I. Edvard

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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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Myoblasts generated by lentiviral mediated MyoD transduction of myotonic dystrophy type 1 von Larsen, Jan, Pettersson, Olof J, Jakobsen, Maria, Thomsen, Rune, Pedersen, Christina B, Hertz, Jens M, Gregersen, Niels, Corydon, Thomas J, Jensen, Thomas G

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Cathepsin K gene mutations and 1q21haplotypes in patients with pycnodysostosis in an outbred population von Haagerup, Annette, Hertz, Jens M, Christensen, Mogens F, Binderup, Helle, Kruse, Torben A

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Apolipoprotein E alleles in mothers of trisomy 18 conceptuses von Hansen, Claus, Bugge, Merete, Brandt, Carsten A, Hertz, Jens M, Tranebjærg, Lisbeth, Mikkelsen, Margareta, Petersen, Michael B

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De Iulio Firmico Materno eiusque in primis de errore profanarum religionum libello :Diss von Hertz, Jens M

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Sind in den Büchern der Könige, Spuren des Pentateuch's und der mosaischen Gesetze zu finden? :Ein Versuch zur Vertheidigung der Bücher der Chronik wie auch des Alterthums der mosa... von Hertz, Jens M

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Full spatial characterization of a nanofocused x-ray free-electron laser beam by ptychographic imaging von Schropp, Andreas, Hoppe, Robert, Meier, Vivienne, Patommel, Jens, Seiboth, Frank, Lee, Hae Ja, Nagler, Bob, Galtier, Eric C., Arnold, Brice, Zastrau, Ulf, Hastings, Jerome B., Nilsson, Daniel, Uhlén, Fredrik, Vogt, Ulrich, Hertz, Hans M., Schroer, Christian G.

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