Unequivocal Delineation of Clinicogenetic Subgroups and Development of a New Model for Improved Outcome Prediction in Neuroblastoma
Vandesompele, Jo, Baudis, Michael, De Preter, Katleen, Van Roy, Nadine, Ambros, Peter, Bown, Nick, Brinkschmidt, Christian, Christiansen, Holger, Combaret, Valérie, Lastowska, Maria, Nicholson, James, O'Meara, Anne, Plantaz, Dominique, Stallings, Raymond, Brichard, Bénédicte, Van den Broecke, Caroline, De Bie, Sylvia, De Paepe, Anne, Laureys, Geneviève, Speleman, Frank
Published in Journal of clinical oncology (01.04.2005)
Published in Journal of clinical oncology (01.04.2005)
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Occipital horn syndrome and classical Menkes Syndrome caused by deep intronic mutations, leading to the activation of ATP7A pseudo-exon
Yasmeen, Saiqa, Lund, Katrine, De Paepe, Anne, De Bie, Sylvia, Heiberg, Arvid, Silva, João, Martins, Márcia, Skjørringe, Tina, Møller, Lisbeth B
Published in European journal of human genetics : EJHG (01.04.2014)
Published in European journal of human genetics : EJHG (01.04.2014)
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Genotype and phenotype analysis of 171 patients referred for molecular study of the fibrillin-1 gene FBN1 because of suspected Marfan syndrome
Loeys, B, Nuytinck, L, Delvaux, I, De Bie, S, De Paepe, A
Published in Archives of internal medicine (1960) (12.11.2001)
Published in Archives of internal medicine (1960) (12.11.2001)
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DUP25 remains unconfirmed
Vermeulen, Stefan J., Menten, Björn, De Bie, Sylvia, Coucke, Paul, Loeys, Bart, Malfait, Fransiska, De Backer, Julie, Speleman, Frank, De Paepe, Anne
Published in American journal of medical genetics. Part A (15.12.2004)
Published in American journal of medical genetics. Part A (15.12.2004)
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Association between Cys282Tyr missense mutation and haptoglobin phenotype polymorphism in patients with chronic hepatitis C
Van Vlierberghe, H, Delanghe, J R, De Bie, S, Praet, M, De Paepe, A, Messiaen, L, De Vos, M, Leroux-Roels, G
Published in European journal of gastroenterology & hepatology (01.09.2001)
Published in European journal of gastroenterology & hepatology (01.09.2001)
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Marfan syndrome in Europe
De Bie, Sylvia, De Paepe, Anne, Delvaux, Isabelle, Davies, Sally, Hennekam, Raoul C M
Published in Community genetics (2004)
Published in Community genetics (2004)
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Refined genetic and physical mapping of BPES type II
Messiaen, L, Leroy, B P, De Bie, S, De Pauw, K, Van Roy, N, Speleman, F, Van Camp, G, De Paepe, A
Published in European journal of human genetics : EJHG (1996)
Published in European journal of human genetics : EJHG (1996)
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Genetic Linkage Between the Collagen Type VII Gene COL7A1 and Pretibial Epidermolysis Bullosa with Lichenoid Features
Naeyaert, Jean Marie, Nuytinck, Lieve, De Bie, Sylvia, Beele, Hilde, Kint, André, De Paepe, Anne
Published in Journal of investigative dermatology (01.05.1995)
Published in Journal of investigative dermatology (01.05.1995)
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Lack of independence between five DNA polymorphisms in the NF1 gene
Messiaen, L, De Bie, S, Moens, T, Van den Enden, A, Leroy, J
Published in Human molecular genetics (01.04.1993)
Published in Human molecular genetics (01.04.1993)
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Fibrillin immunofluorescence in pseudoxanthoma elasticum
Godfrey, Maurice, Cisler, Jason, Geerts, Marie-Louise, Christiano, Angela, Uitto, Jouni, Bie, Sylvia De, DePaepe, Anne
Published in Journal of the American Academy of Dermatology (01.04.1995)
Published in Journal of the American Academy of Dermatology (01.04.1995)
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Marfan Syndrome in Europe: A Questionnaire Study on Patient Perceptions
De Bie, Sylvia, De Paepe, Anne, Delvaux, Isabelle, Davies, Sally, Hennekam, Raoul C.M.
Published in Community genetics (01.01.2004)
Published in Community genetics (01.01.2004)
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Familial dermatoglyphic analysis in syndactyly type I
Matton, M, De Bie, S, Anseeuw, A
Published in The Journal of hand surgery (American ed.) (01.11.1981)
Published in The Journal of hand surgery (American ed.) (01.11.1981)
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Pseudoxanthoma elasticum: similar autosomal recessive subtype in Belgian and Afrikaner families
De Paepe, A, Viljoen, D, Matton, M, Beighton, P, Lenaerts, V, Vossaert, K, De Bie, S, Voet, D, De Laey, J J, Kint, A
Published in American journal of medical genetics (01.01.1991)
Published in American journal of medical genetics (01.01.1991)
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