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Marcelis C 1
Showing records 1 to 1 | Display all abstracts from Marcelis C22051 Identification of entire LMX1B gene deletions in nail patella syndrome: Evidence for haploinsufficiency as the main pathogenic mechanism underlying dominant inheritance in man
Bongers EMHF; de Wijs IJ; Marcelis C; Hoefsloot LH; Knoers NVAM
European Journal of Human Genetics 2008; 16: 1240-1244
