Résultats de la recherche

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(1 - 9 of 9)
Osteosclerotic bone dysplasia in siblings with a Fam20C mutation
Long-term follow-up and molecular characterization of a patient with a RECQL4 mutation spectrum disorder
Neural tube defects: the experience of the registry of congenital malformations of Alsace, France, 1995-2009
Molecular diagnosis reveals genetic heterogeneity for the overlapping MKKS and BBS phenotypes
Épidémiologie des fentes labio-palatines : expérience du Registre de malformations congénitales d’Alsace entre 1995 et 2006 [Epidemiology of orofacial clefts (1995-2006) in France (Congenital Malformations of Alsace Registry)]

Islandora displays