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Page 1
Chromosome aberrations in fibrous dysplasia.
Dal Cin P, Sciot R, Speleman F, Samson I, Laureys G, de Potter C, Meire F, van Damme B, van den Berghe H. Dal Cin P, et al. Among authors: meire f. Cancer Genet Cytogenet. 1994 Oct 15;77(2):114-7. doi: 10.1016/0165-4608(94)90225-9. Cancer Genet Cytogenet. 1994. PMID: 7954320
Cohen syndrome: the clinical symptoms and stigmata at a young age.
Fryns JP, Legius E, Devriendt K, Meire F, Standaert L, Baten E, Van den Berghe H. Fryns JP, et al. Among authors: meire f. Clin Genet. 1996 May;49(5):237-41. doi: 10.1111/j.1399-0004.1996.tb03780.x. Clin Genet. 1996. PMID: 8832131
Retinal manifestations in fibromuscular dysplasia.
Meire FM, De Laey JJ, Van Thienen MN, Schuddinck L. Meire FM, et al. Eur J Ophthalmol. 1991 Apr-Jun;1(2):63-8. doi: 10.1177/112067219100100202. Eur J Ophthalmol. 1991. PMID: 1821202
Osteoporosis-pseudoglioma syndrome.
De Paepe A, Leroy JG, Nuytinck L, Meire F, Capoen J. De Paepe A, et al. Among authors: meire f. Am J Med Genet. 1993 Jan 1;45(1):30-7. doi: 10.1002/ajmg.1320450110. Am J Med Genet. 1993. PMID: 8418655
Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome.
Beysen D, Raes J, Leroy BP, Lucassen A, Yates JR, Clayton-Smith J, Ilyina H, Brooks SS, Christin-Maitre S, Fellous M, Fryns JP, Kim JR, Lapunzina P, Lemyre E, Meire F, Messiaen LM, Oley C, Splitt M, Thomson J, Van de Peer Y, Veitia RA, De Paepe A, De Baere E. Beysen D, et al. Among authors: meire f. Am J Hum Genet. 2005 Aug;77(2):205-18. doi: 10.1086/432083. Epub 2005 Jun 16. Am J Hum Genet. 2005. PMID: 15962237 Free PMC article.
119 results