em. prof. dr. Juliaan Leroy
Show
Sort by
-
Deficient decorin biosynthesis in the neonatal progeroid syndrome'. Chapter 24 in 'Dysmorphology and Genetics of Cardiovascular Disorders', Bartsocas CS, Beighton P., Eds., HTA Medical Publications, Athens, 1994, pp 166-176.
-
Disorders of lysosomal enzymes. Chapter 23 in 'Connective tissue and its heritable Disorders'. Royce P.M. and Steinmann B., eds., Wiley-Liss, New York, 1992, pp. 613-639.
-
Substitution of Gly 769 by serine in collagen type III in a three generation family showing variable expressivity of EDS type IV. Proceed. 5th Internat. Conference on osteogenesis imperfecta, 1993, pp. 114-115.
-
Hoofdstuk 22 in Codex Medicus, E. Eyskens, L. Feenstra, A.E. Meinders en J.P. Vandenbroucke, Eds., 10e druk, Elsevier, Arnhem, pp. 799-817.
-
Medische Genetica en moleculaire Biologie. (1996).
-
The mucolipidoses (including I-cell disease). Chapter 19 in Handbook of Clinical Neurology. Vol. 66, Revised Series 22, Neurodystrophies and Neurolipidoses, P.J. Vinken, G.W. Bruyn, H.W. Moser, Eds., Elsevier, Amsterdam, pp. 377-387, 1996.
-
Oligosaccharidoses.
-
Chapter 97 in 'Emery and Rimoin's Principles and Practice of Medical Genetics'. D.L. Rimoin, J.M. Connor, R.E. Pyeritz, eds., 3rd Edit., Churchill Livingstone, New York, pp. 2O81-2103, 1996.