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Pierre Maroteaux - bibliography

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Biography

French paediatrician, born 1926, Versailles.

Bibliography

  • Les maladies osseuses de l'enfant.
    With Clement Fauré, Claude Fessard and Pierre Rigault.
    Foreword by Maurice Lamy.
    In the series: Flammarion médecine-sciences.
    1974. 1982. 3rd edition, 619 pages, 1995.
    4th edition, 482 pages, by Pierre Maroteaux and Martine Le Merrer. 2002.
  • Bone diseases of children.
    With Clement Fauré, Claude Fessard and Pierre Rigault.
    A translation of: Les maladies osseuses de l'enfant.
    Translated and adopted by Herbert J. Kaufmann.
    Philadelphia : Lippincott, 1979, 17 + 435 pages.
  • Les formes pseudoachondroplastiques des dysplasies spondyloepiphysaires.
    P. Maroteaux, M. Lamy.
    La presse médicale, Paris, 1959, 67: 383-386.
  • Hydrocephalus and achondroplasia. A study of 25 observations.
    A. Pierre-Kahn, J. F. Hirsch, D. Renier, J. Metzger, P. Maroteaux.
    Child's Brain, 1980, 7: 205-19
  • Bone Disorders of Children.
    Oxford Monographs of Medical Genetics, No 23, 1993.
  • Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia.
    F. Rousseau, J. Bonaventure, L. Legeai-Mallet, A. Pelet, J. M. Rozet, P. Maroteaux, M. LeMerrer, and A. Munnich.
    Nature, London, 1994, 371: 252-254.
  • Cerebro-costo-mandibular syndrome: a follow-up study with 6 patients.
    C. Schrander-Stumpel C, S. van der Meer, C. de Die-Smulders, P. Meinecke, E. Rupprecht, P. Maroteaux, J. Schranders, J. P. Fryns.
    Genetic Counseling, 1996, 7: 71-72
  • Mutations of the fibroblast growth factor receptor-3 gene in achondroplasia.
    F. Rousseau, J. Bonaventure, L. Legeai-Mallet, A. Pelet, J. M. Rozet, P. Maroteaux, M. LeMerrer, and A. Munnich,.
    Hormone Research, 1996, 45:108-110.
  • An extension of the admixture test for the study of genetic heterogeneity in hereditary multiple exostoses.
    Laurence Legeai-Mallet, Patricia Margaritte-Jeannin, Mohamed Lemdani, M. Le Merrer, Henry Plauchu, Pierre Maroteaux, A. Munnich, Françoise Clerget-Darpoux.
    Human Genetics, Berlin, 1997, Volume 99 Issue 3, pp 298-302.
  • Presentation of six cases of Stüve-Wiedemann syndrome.
    Valérie Cormier-Daire, A. Munnich, Stanislas Lyonnet, Pierre Rustin, Anne-Lise Delezoide, Pierre Maroteaux, Martine Le Merrer.
    Pediatric Radiology, Berlin, 1998, Volume 28 Issue 10, pp 776-780.

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