Revisiting metatropic dysplasia: Presentation of a series of 19 novel patients and review of the literature von Geneviève, D., Le Merrer, M., Feingold, J., Munnich, A., Maroteaux, P., Cormier-Daire, V.

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Du danger d'être petit. Une taille inférieure à la moyenne devient-elle pathologique dans notre société ? von MAROTEAUX, P

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The danger of small height. Does a lower height become pathological in our society? von Maroteaux, P

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Brachytelephalangic chondrodysplasia punctata: a possible X-linked recessive form von MAROTEAUX, P

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Clinical and genetic heterogeneity of hypochondroplasia von Rousseau, F, Bonaventure, J, Legeai-Mallet, L, Schmidt, H, Weissenbach, J, Maroteaux, P, Munnich, A, Le Merrer, M

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Clinical, radiological, and chondro-osseous findings in opsismodysplasia: survey of a series of 12 unreported cases von Cormier-Daire, V, Delezoide, A L, Philip, N, Marcorelles, P, Casas, K, Hillion, Y, Faivre, L, Rimoin, D L, Munnich, A, Maroteaux, P, Le Merrer, M

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Acromicric dysplasia: long term outcome and evidence of autosomal dominant inheritance von Faivre, L, Le Merrer, M, Baumann, C, Polak, M, Chatelain, P, Sulmont, V, Cousin, J, Bost, M, Cordier, M P, Zackai, E, Russell, K, Finidori, G, Pouliquen, J C, Munnich, A, Maroteaux, P, Cormier-Daire, V

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Homozygosity mapping of a Desbuquois dysplasia locus to chromosome 17q25.3 von Faivre, L, Le Merrer, M, Al-Gazali, L I, Ausems, M G E M, Bitoun, P, Bacq, D, Maroteaux, P, Munnich, A, Cormier-Daire, V

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Long-term follow-up in a patient with metatropic dysplasia von Geneviève, D., Le Merrer, M., Munnich, A., Maroteaux, P., Cormier-Daire, V.

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Mauro Baschirotto annual Award in human genetics. The speech of acceptance by Professor Maroteaux. Thoughts of a geneticist von Maroteaux, P

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Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia von Rousseau, Francis, Bonaventure, Jacky, Legeai-Mallet, Laurence, Pelet, Anna, Rozet, Jean-Michel, Maroteaux, Pierre, Merrer, Martine Le, Munnich, Arnold

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Mutations in three subdomains of the carboxy-terminal region of collagen type X account for most of the Schmid metaphyseal dysplasias von BONAVENTURE, J, CHAMINADE, F, MAROTEAUX, P

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Exclusion of chromosome 9 helps to identify mild variants of acromesomelic dysplasia Maroteaux type von Faivre, Laurence, Le Merrer, Martine, Megarbane, André, Gilbert, Brigitte, Mortier, Geert, Cusin, Veronica, Munnich, Arnold, Maroteaux, Pierre, Cormier-Daire, Valérie

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International classification of osteochondrodysplasias von Beighton, P., Giedion, A., Gorlin, R., Hall, J., Horton, B., Kozlowski, K., Lachman, R., Langer, L. O., Maroteaux, P., Poznanski, A., Rimoin, D. L., Sillence, D., Spranger, J.

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The spondylometaphyseal dysplasias : a tentative classification von MAROTEAUX, P, SPRANGER, J

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Du danger d’être petit von Maroteaux, P.

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ÉTUDE GÉNÉTIQUE DU GARGOYLISME von Lamy, M., Maroteaux, P., Bader, J.-P.

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Enfant battu ou enfant fragile ? von Maroteaux, P, Le Merrer, M

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A cluster of sulfatase genes on Xp22.3: Mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy von Franco, Brunella, Meroni, Germana, Parenti, Giancarlo, Levilliers, Jacqueline, Bernard, Loris, Gebbia, Marinella, Cox, Liza, Maroteaux, Pierre, Sheffield, Leslie, Rappold, Gudrun A, Andria, Generoso, Petit, Christine, Ballabio, Andrea

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Unusual fan shaped ossification in a female fetus with radiological features of boomerang dysplasia von Odent, Sylvie, Loget, Philippe, Le Marec, Bernard, Delezoïde, Anne-Lise, Maroteaux, Pierre

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