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Displaying 16 results.
    • Journal article
    Neural-tube Defects and Omphalocele in Trisomy-18
    Vanmaldergem, L. Gillerot, Y. Koulischer, L. (1989) Clinical Genetics : an international journal of genetics and molecular medicine — Vol. 35, no. 1, p. 77-78 (1989)
    • Journal article
    Microspherophakia-metaphyseal Dysplasia - a New Dominantly Inherited Bone Dysplasia With Severe Eye Involvement
    Verloes, A. Vanmaldergem, L. Demarneffe, P. Dufier, JL. Maroteaux, P. (1990) Journal of Medical Genetics : an international peer-reviewed journal for health professionals and researchers in all areas of genetics — Vol. 27, no. 7, p. 467-471 (1990)
    • Journal article
    Mental-retardation, Short Stature, Almond-shaped Eyes, Small Downturned Mouth and Coned Epiphyses - a New Case of Hunter-fraser Syndrome
    Vanmaldergem, L. Gillerot, Y. Perlmutter, N. Wetzburger, C. Koulischer, L. (1990) American Journal of Medical Genetics — Vol. 37, no. 2, p. 283-285 (1990)
    • Journal article
    Trisomy 20q - a New Case and Further Phenotypic Delineation
    Herens, C. Verloes, A. Laloux, F. Vanmaldergem, L. (1990) Clinical Genetics : an international journal of genetics and molecular medicine — Vol. 37, no. 5, p. 363-366 (1990)
    • Journal article
    Symptomatic Similarities in 3 Syndromes - Reply
    Vanmaldergem, L. (1989) American Journal of Medical Genetics — Vol. 34, no. 4, p. 612-612 (1989)
    • Journal article
    Oral-facial-digital Syndrome Type-i in a Newborn Male
    Gillerot, Y. Heimann, M. Fourneau, C. Dumoulin, Christine[UCL] Vanmaldergem, L. (1993) American Journal of Medical Genetics — Vol. 46, no. 3, p. 335-338 (1993)
    • Journal article
    Facial Anomalies in Congenital Cutis Laxa With Retarded Growth and Skeletal Dysplasia
    Vanmaldergem, L. Ogur, G. Yuksel, M. (1989) American Journal of Medical Genetics — Vol. 32, no. 2, p. 265-265 (1989)
    • Speech
    Genetics of the Berardinelli-Seip syndrome (congenital generalized lipodystrophy) in Norway: Epidemiology and gene mapping
    GeddeDahl, T Trygstad, O Vanmaldergem, L. Magre, J vanderHagen, C Olaisen, B Stenersen, M Mevag, B Copeau, J DesboisMouthon, C Vigouroux, C. Hilbert, P Faure, S Weissenbach, J (1996) Symposium on Generalized Lipodystrophy, Congenital (Berardinelli-Seip Syndrome) and Acquired (Lipoatrophy, Seip-Lawrence Syndrome) — OSLO(Norway)
    • Journal article
    Increased Prostacyclin Biosynthesis in a Patient With Homocystinuria
    Vanmaldergem, L. Capel, P. Boeynaems, JM. (1990) European Journal of Pediatrics — Vol. 149, no. 9, p. 666-667 (1990)
    • Journal article
    Roberts-sc Phocomelia Syndrome With Exencephaly
    Verloes, A. Herens, C. Vanmaldergem, L. Retz, MC. Dodinval, P. (1989) Annales de génétique — Vol. 32, no. 3, p. 169-170 (1989)
    • Journal article
    Peroxisomal Localization of the Immunoreactive Beta-oxidation Enzymes in a Neonate With a Beta-oxidation Defect - Pathological Observations in Liver, Adrenal-cortex and Kidney
    Espeel, M. Roels, F. Vanmaldergem, L. Decraemer, D. Dacremont, G. Wanders, RJA. Hashimoto, T. (1991) Virchows Archiv. Section A: Pathological Anatomy and Histopathology — Vol. 419, no. 4, p. 301-308 (1991)
    • Journal article
    Mapping the RP2 locus for X-linked retinitis pigmentosa on proximal Xp: A genetically defined 5-cM critical region and exclusion of candidate genes by physical mapping
    Thiselton, DL Hampson, RM Nayudu, M Vanmaldergem, L. Wolf, ML Saha, BK Bhattacharya, SS Hardcastle, AJ (1996) PCR Methods and Applications — Vol. 6, no. 11, p. 1093-1102 (1996)
    • Journal article
    Primordial Osteodysplastic Dwarfism Type-i in Association With Corneal Clouding - Evidence for Autosomal Recessive Inheritance
    Vanmaldergem, L. Gillerot, Y. Godhaird, M. Nemec, E. Koulischer, L. (1990) Clinical Genetics : an international journal of genetics and molecular medicine — Vol. 38, no. 5, p. 359-361 (1990)
    • Journal article
    Nonimmune Hydrops Fetalis Associated With Genetic Abnormalities
    Jauniaux, E. Vanmaldergem, L. Demunter, C. Moscoso, G. Gillerot, Y. (1990) Obstetrics and Gynecology — Vol. 75, no. 3, p. 568-572 (1990)
    • Journal article
    Lethal Short-rib With Median Cleft and Without Polydactyly - a Fourth Case
    Vanmaldergem, L. Gillerot, Y. Salmin, E. Verloes, A. Koulischer, L. (1990) Pediatric Radiology : roentgenology, nuclear medicine, ultrasonics, CT, MRI — Vol. 20, no. 5, p. 367-368 (1990)
    • Journal article
    The Gene for Hereditary Multiple Exostoses Does Not Map To the Langer-giedion Region (8q23-q24)
    Lemerrer, M. Benothmane, K. Stanescu, V. Lyonnet, S. Vanmaldergem, L. Royer, G. Munnich, A. Maroteaux, P. (1992) Journal of Medical Genetics : an international peer-reviewed journal for health professionals and researchers in all areas of genetics — Vol. 29, no. 10, p. 713-715 (1992)