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Results: 1-5 |
Results: 5

Authors: Leroy, JG Seppala, R Huizing, M Dacremont, G De Simpel, H Van Coster, RN Orvisky, E Krasnewich, DM Gahl, WA
Citation: Jg. Leroy et al., Dominant inheritance of sialuria, an inborn error of feedback inhibition, AM J HU GEN, 68(6), 2001, pp. 1419-1427

Authors: Speleman, F Callens, B Logghe, K Van Roy, N Horsley, SW Jauch, A Verschraegen-Spae, MR Leroy, JG
Citation: F. Speleman et al., Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35 -> qter: Molecular cytogenetic analysis and clinical phenotype intwo generations, AM J MED G, 93(5), 2000, pp. 349-354

Authors: Mortier, G Nuytinck, L Craen, M Renard, JP Leroy, JG De Paepe, A
Citation: G. Mortier et al., Clinical and radiographic features of a family with hypochondroplasia owing to a novel Asn540Ser mutation in the fibroblast growth factor receptor 3 gene, J MED GENET, 37(3), 2000, pp. 220-224

Authors: Loeys, BL Van Coster, RN Defreyne, LR Leroy, JG
Citation: Bl. Loeys et al., Fungal intracranial aneurysm in a child with familial chronic mucocutaneous candidiasis, EUR J PED, 158(8), 1999, pp. 650-652

Authors: Loeys, BL Lemmerling, MM Van Mol, CE Leroy, JG
Citation: Bl. Loeys et al., The Meier-Gorlin syndrome, or ear patella short stature syndrome, in sibs, AM J MED G, 84(1), 1999, pp. 61-67
Risultati: 1-5 |