Deficiency of the Cytoskeletal Protein SPECC1L Leads to Oblique Facial Clefting
Saadi, Irfan, Alkuraya, Fowzan S., Gisselbrecht, Stephen S., Goessling, Wolfram, Cavallesco, Resy, Turbe-Doan, Annick, Petrin, Aline L., Harris, James, Siddiqui, Ursela, Grix, Arthur W., Hove, Hanne D., Leboulch, Philippe, Glover, Thomas W., Morton, Cynthia C., Richieri-Costa, Antonio, Murray, Jeffrey C., Erickson, Robert P., Maas, Richard L.
Published in American journal of human genetics (15.07.2011)
Published in American journal of human genetics (15.07.2011)
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Journal Article
Biomechanical properties of the patellar tendon in children with heritable connective tissue disorders
Jensen, Jacob K., Nygaard, Rie H., Svensson, Rene B., Hove, Hanne D., Magnusson, S. Peter, Kjær, Michael, Couppé, Christian
Published in European journal of applied physiology (01.07.2018)
Published in European journal of applied physiology (01.07.2018)
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Facial Asymmetry in Children with Unicoronal Synostosis who have Undergone Craniofacial Reconstruction in Infancy
Öwall, Louise, Darvann, Tron A., Larsen, Per, Hove, Hanne D., Hermann, Nuno V., Bøgeskov, Lars, Kreiborg, Sven
Published in The Cleft palate-craniofacial journal (01.07.2016)
Published in The Cleft palate-craniofacial journal (01.07.2016)
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Journal Article
Craniofacial morphology in Muenke syndrome
Keller, Mette K, Hermann, Nuno V, Darvann, Tron A, Larsen, Per, Hove, Hanne D, Christensen, Leif, Schwartz, Marianne, Marsh, Jeffrey L, Kreiborg, Sven
Published in The Journal of craniofacial surgery (01.03.2007)
Published in The Journal of craniofacial surgery (01.03.2007)
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Journal Article
Monozygotic twins presenting with isolated sagittal and bicoronal synostosis, respectively
Hove, Hanne D, Dunø, Morten, Larsen, Per, Kreiborg, Sven
Published in Clinical dysmorphology (01.04.2016)
Published in Clinical dysmorphology (01.04.2016)
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Journal Article
The Cardiac Phenotype in Patients With a CHD7 Mutation
Corsten-Janssen, Nicole, Kerstjens-Frederikse, Wilhelmina S, du Marchie Sarvaas, Gideon J, Baardman, Maria E, Bakker, Marian K, Bergman, Jorieke E.H, Hove, Hanne D, Heimdal, Ketil R, Rustad, Cecilie F, Hennekam, Raoul C.M, Hofstra, Robert M.W, Hoefsloot, Lies H, Van Ravenswaaij-Arts, Conny M.A, Kapusta, Livia
Published in Circulation. Cardiovascular genetics (01.06.2013)
Published in Circulation. Cardiovascular genetics (01.06.2013)
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Journal Article
Microdeletion in distal 17p13.1: A recognizable phenotype with microcephaly, distinctive facial features, and intellectual disability
Zeesman, Susan, Kjaergaard, Susanne, Hove, Hanne D., Kirchhoff, Maria, Stevens, Jadd M., Nowaczyk, Małgorzata J.M.
Published in American journal of medical genetics. Part A (01.08.2012)
Published in American journal of medical genetics. Part A (01.08.2012)
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Journal Article
Automated quantification and analysis of mandibular asymmetry
Darvann, Tron A, Hermann, Nuno V, Larsen, Per, Ólafsdóttir, Hildur, Hansen, Izabella V, Hove, Hanne D, Christensen, Leif, Rueckert, Daniel, Kreiborg, Sven
Published in 2010 IEEE International Symposium on Biomedical Imaging: From Nano to Macro (01.04.2010)
Published in 2010 IEEE International Symposium on Biomedical Imaging: From Nano to Macro (01.04.2010)
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Conference Proceeding
A study of the clinical and radiological features in a cohort of 93 patients with a COL2A1 mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype
Terhal, Paulien A., Nievelstein, Rutger Jan A. J., Verver, Eva J. J., Topsakal, Vedat, van Dommelen, Paula, Hoornaert, Kristien, Le Merrer, Martine, Zankl, Andreas, Simon, Marleen E. H., Smithson, Sarah F., Marcelis, Carlo, Kerr, Bronwyn, Clayton-Smith, Jill, Kinning, Esther, Mansour, Sahar, Elmslie, Frances, Goodwin, Linda, van der Hout, Annemarie H., Veenstra-Knol, Hermine E., Herkert, Johanna C., Lund, Allan M., Hennekam, Raoul C. M., Mégarbané, André, Lees, Melissa M., Wilson, Louise C., Male, Alison, Hurst, Jane, Alanay, Yasemin, Annerén, Göran, Betz, Regina C., Bongers, Ernie M. H. F., Cormier-Daire, Valerie, Dieux, Anne, David, Albert, Elting, Mariet W., van den Ende, Jenneke, Green, Andrew, van Hagen, Johanna M., Hertel, Niels Thomas, Holder-Espinasse, Muriel, den Hollander, Nicolette, Homfray, Tessa, Hove, Hanne D., Price, Susan, Raas-Rothschild, Annick, Rohrbach, Marianne, Schroeter, Barbara, Suri, Mohnish, Thompson, Elizabeth M., Tobias, Edward S., Toutain, Annick, Vreeburg, Maaike, Wakeling, Emma, Knoers, Nine V., Coucke, Paul, Mortier, Geert R.
Published in American journal of medical genetics. Part A (01.03.2015)
Published in American journal of medical genetics. Part A (01.03.2015)
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Journal Article
Deficiency of the Cytoskeletal Protein SPECC1 L Leads to Oblique Facial Clefting
SAADI, Irfan, ALKURAYA, Fowzan S, HOVE, Hanne D, LEBOULCH, Philippe, GLOVER, Thomas W, MORTON, Cynthia C, RICHIERI-COSTA, Antonio, MURRAY, Jeffrey C, ERICKSON, Robert P, MAAS, Richard L, GISSELBRECHT, Stephen S, GOESSLING, Wolfram, CAVALLESCO, Resy, TURBE-DOAN, Annick, PETRIN, Aline L, HARRIS, James, SIDDIQUI, Ursela, GRIX, Arthur W
Published in American journal of human genetics (2011)
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Published in American journal of human genetics (2011)
Journal Article