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1by Fransen, Erik, Valgaeren, Hanne, Janssens, Katleen, Sommen, Manou, De Ridder, Raphael, Vandeweyer, Geert, Bisceglia, Luigi, Soler, Vincent, Hoischen, Alexander, Mortier, Geert, Malecaze, François, Koppen, Carina, Van Camp, GuyGet full text
Published in European journal of human genetics : EJHG
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2by Højland, Allan Thomas, Tavernier, Lisse J. M., Schrauwen, Isabelle, Sommen, Manou, Topsakal, Vedat, Schatteman, Isabelle, Dhooge, Ingeborg, Huber, Alex, Zanetti, Diego, Kunst, Henricus P. M., Hoischen, Alexander, Petersen, Michael B., Van Camp, Guy, Fransen, ErikGet full text
Published in Human genetics
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3A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairmentby SCHRAUWEN, Isabelle, HELFMANN, Sarah, DHEEDENE, Annelies, CLAES, Charlotte, FRANSEN, Erik, HASHEMZADEH CHALESHTORI, Morteza, COUCKE, Paul, LEE, Amy, MOSER, Tobias, VAN CAMP, Guy, INAGAKI, Akira, PREDOEHL, Friederike, AMIN TABATABAIEFAR, Mohammad, MAGDALENA PICHER, Maria, SOMMEN, Manou, ZAZO SECO, Celia, OOSTRIK, Jaap, KREMER, HannieGet full text
Published in American journal of human genetics
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5Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6by Ratbi, Ilham, Falkenberg, Kim D., Sommen, Manou, Al-Sheqaih, Nada, Guaoua, Soukaina, Vandeweyer, Geert, Urquhart, Jill E., Chandler, Kate E., Williams, Simon G., Roberts, Neil A., El Alloussi, Mustapha, Black, Graeme C., Ferdinandusse, Sacha, Ramdi, Hind, Heimler, Audrey, Fryer, Alan, Lynch, Sally-Ann, Cooper, Nicola, Ong, Kai Ren, Smith, Claire E.L., Inglehearn, Christopher F., Mighell, Alan J., Elcock, Claire, Poulter, James A., Tischkowitz, Marc, Davies, Sally J., Sefiani, Abdelaziz, Mironov, Aleksandr A., Newman, William G., Waterham, Hans R., Van Camp, GuyGet full text
Published in American journal of human genetics
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6by Valgaeren, Hanne, Sommen, Manou, Beyens, Matthias, Vandeweyer, Geert, Schrauwen, Isabelle, Schepers, Anne, Schatteman, Isabelle, Topsakal, Vedat, Dhooge, Ingeborg, Kunst, Henricus, Zanetti, Diego, Huber, Alexander M., Hoischen, Alexander, Fransen, Erik, Van Camp, GuyGet full text
Published in Molecular genetics and genomics : MGG
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7by Schrauwen, Isabelle, Valgaeren, Hanne, Tomas-Roca, Laura, Sommen, Manou, Altunoglu, Umut, Wesdorp, Mieke, Beyens, Matthias, Fransen, Erik, Nasir, Abdul, Vandeweyer, Geert, Schepers, Anne, Rahmoun, Malika, van Beusekom, Ellen, Huentelman, Matt J, Offeciers, Erwin, Dhooghe, Ingeborg, Huber, Alex, Van de Heyning, Paul, Zanetti, Diego, De Leenheer, Els M R, Gilissen, Christian, Hoischen, Alexander, Cremers, Cor W, Verbist, Berit, de Brouwer, Arjan P M, Padberg, George W, Pennings, Ronald, Kayserili, Hülya, Kremer, Hannie, Van Camp, Guy, van Bokhoven, HansGet full text
Published in Genetics in medicine
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