SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)

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Laser Capture Microdissection of Mouse Embryonic Cartilage and Bone for Gene Expression Analysis
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V Belin1, V Cusin, G Viot

  • 1Département de Génétique et Unité de Recherches sur les Handicaps Génétiques de l'Enfant INSERM U393, Hôpital des Enfants Malades, Paris, France.

Nature Genetics
|May 20, 1998
PubMed

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