De Bie S - Search Results

1

Refined genetic and physical mapping of BPES type II.

Messiaen L, Leroy BP, De Bie S, De Pauw K, Van Roy N, Speleman F, Van Camp G, De Paepe A. Messiaen L, et al. Among authors: de paepe a, de pauw k, de bie s. Eur J Hum Genet. 1996;4(1):34-8. doi: 10.1159/000472167. Eur J Hum Genet. 1996. PMID: 8800926

2

Kallmann syndrome in a patient with congenital spherocytosis and an interstitial 8p11.2 deletion.

Vermeulen S, Messiaen L, Scheir P, De Bie S, Speleman F, De Paepe A. Vermeulen S, et al. Among authors: de paepe a, de bie s. Am J Med Genet. 2002 Apr 1;108(4):315-8. doi: 10.1002/ajmg.10295. Am J Med Genet. 2002. PMID: 11920837

3

Genetic counseling of a couple presenting respectively terminal transverse defects and congenital arthrogryposis.

De Paepe A, De Bie S. De Paepe A, et al. Among authors: de bie s. Genet Couns. 1991;2(4):195-203. Genet Couns. 1991. PMID: 1799416

4

Genetic linkage between the collagen type VII gene COL7A1 and pretibial epidermolysis bullosa with lichenoid features.

Naeyaert JM, Nuytinck L, De Bie S, Beele H, Kint A, De Paepe A. Naeyaert JM, et al. Among authors: de paepe a, de bie s. J Invest Dermatol. 1995 May;104(5):803-5. doi: 10.1111/1523-1747.ep12606999. J Invest Dermatol. 1995. PMID: 7738360 Free article.

5

Lack of independence between five DNA polymorphisms in the NF1 gene.

Messiaen L, De Bie S, Moens T, Van den Enden A, Leroy J. Messiaen L, et al. Among authors: de bie s. Hum Mol Genet. 1993 Apr;2(4):485. doi: 10.1093/hmg/2.4.485. Hum Mol Genet. 1993. PMID: 8504312 No abstract available.

6

Occipital horn syndrome and classical Menkes Syndrome caused by deep intronic mutations, leading to the activation of ATP7A pseudo-exon.

Yasmeen S, Lund K, De Paepe A, De Bie S, Heiberg A, Silva J, Martins M, Skjørringe T, Møller LB. Yasmeen S, et al. Among authors: de paepe a, de bie s. Eur J Hum Genet. 2014 Apr;22(4):517-21. doi: 10.1038/ejhg.2013.191. Epub 2013 Sep 4. Eur J Hum Genet. 2014. PMID: 24002164 Free PMC article.

7

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 JJ, Kint A. De Paepe A, et al. Among authors: de laey jj, de bie s. Am J Med Genet. 1991 Jan;38(1):16-20. doi: 10.1002/ajmg.1320380105. Am J Med Genet. 1991. PMID: 2012127

8

Carrier screening for cystic fibrosis in a prenatal setting.

Delvaux I, van Tongerloo A, Messiaen L, Van Loon C, De Bie S, Mortier G, De Paepe A. Delvaux I, et al. Among authors: de paepe a, de bie s. Genet Test. 2001 Summer;5(2):117-25. doi: 10.1089/109065701753145574. Genet Test. 2001. PMID: 11551097

9

Unequivocal delineation of clinicogenetic subgroups and development of a new model for improved outcome prediction in neuroblastoma.

Vandesompele J, Baudis M, De Preter K, Van Roy N, Ambros P, Bown N, Brinkschmidt C, Christiansen H, Combaret V, Lastowska M, Nicholson J, O'Meara A, Plantaz D, Stallings R, Brichard B, Van den Broecke C, De Bie S, De Paepe A, Laureys G, Speleman F. Vandesompele J, et al. Among authors: de paepe a, de preter k, de bie s. J Clin Oncol. 2005 Apr 1;23(10):2280-99. doi: 10.1200/JCO.2005.06.104. J Clin Oncol. 2005. PMID: 15800319 Free article.

10

Marfan syndrome in Europe.

De Bie S, De Paepe A, Delvaux I, Davies S, Hennekam RC. De Bie S, et al. Among authors: de paepe a. Community Genet. 2004;7(4):216-25. doi: 10.1159/000082265. Community Genet. 2004. PMID: 15692197

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