Browsing by Author "Maari, C."
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Lack of genotype-phenotype correlation for Kindlin-1 mutations in Kindler syndrome and evidence for possible genetic heterogeneity
Lai-Cheong, J.; Liu, L.; Taskesen, M.; Akdeniz, S.; Maari, C.; Emanuel, P.; McGrath, J. A. (Wiley-Blackwell, 2008)[Abstract Not Available]
