Søgeresultater - Niels Tommerup
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Occurrence of cancer in women with Turner syndrome af Henrik Hasle, Jørgen H. Olsen, Jørgen Nielsen, Jan Hansen, U Friedrich, Niels Tommerup
Udgivet 1996Artigo -
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The Human Intrinsic Factor-Vitamin B12 Receptor,Cubilin: Molecular Characterization and Chromosomal Mapping of the Gene to 10p Within the Autosomal Recessive Megaloblastic Anemia (... af Renata Kozyraki, Mette Kristiansen, Asli Silahtaroglu, Claus Hansen, Christian Jacobsen, Niels Tommerup, P Verroust, Søren K. Moestrup
Udgivet 1998Artigo -
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Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome af J.M. Belloso, Iben Bache, Míriam Guitart, M.R. Caballı́n, Christina Halgren, Maria Kirchhoff, Hans‐Hilger Ropers, Niels Tommerup, Zeynep Tümer
Udgivet 2007Artigo -
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Heterogeneous Nuclear Ribonucleoproteins H, H′, and F Are Members of a Ubiquitously Expressed Subfamily of Related but Distinct Proteins Encoded by Genes Mapping to Different Chrom... af Bent Honoré, Hugo Hanne, Vorum Henrik, Dejgaard Kurt, Liu Xiangdang, Gromov Pavel, Peder Madsen, Gesser Borbala, Niels Tommerup, E. Celis Julio
Udgivet 1995Artigo -
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Molecular Characterization of a Novel Human Hybrid-type Receptor That Binds the α2-Macroglobulin Receptor-associated Protein af Linda Jacobsen, Peder Madsen, Søren K. Moestrup, Anders H. Lund, Niels Tommerup, Anders Nykjær, Lars Sottrup‐Jensen, Jørgen Gliemann, Claus M. Petersen
Udgivet 1996Artigo -
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The segregation of different submicroscopic imbalances underlying the clinical variability associated with a familial karyotypically balanced translocation af Ana Carolina Fonseca, Adriano Bonaldi, Simone Aparecida Siqueira Fonseca, Paulo Alberto Otto, Fernando Kok, Mads Bak, Niels Tommerup, Angela Maria Vianna‐Morgante
Udgivet 2015Artigo -
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A Molecular Analysis of the Yemenite Deaf-Blind Hypopigmentation Syndrome: SOX10 Dysfunction Causes Different Neurocristopathies af Nadège Bondurand, Kirsten Kuhlbrodt, Véronique Pingault, Janna Enderich, M. Sajus, Niels Tommerup, Mette Warburg, Raoul C. M. Hennekam, Andrew Read, Michael Wegner, Michel Goossens
Udgivet 1999Artigo -
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A Functional Link between the Histone Demethylase PHF8 and the Transcription Factor ZNF711 in X-Linked Mental Retardation af Daniela Kleine‐Kohlbrecher, Jesper Frank Christensen, Julien Vandamme, Iratxe Abarrategui, Mads Bak, Niels Tommerup, Xiaobing Shi, Or Gozani, Juri Rappsilber, Anna Elisabetta Salcini, Kristian Helin
Udgivet 2010Artigo -
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Mesomelia-synostoses syndrome: contiguous deletion syndrome, SULF1 haploinsufficiency or enhancer adoption? af Ingrid Bendas Feres Lima, Lúcia de Fátima Marques de Moraes, Carlos Roberto da Fonseca, Juan Clinton Llerena, Mana M. Mehrjouy, Niels Tommerup, Elenice Ferreira Bastos
Udgivet 2024Artigo
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