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Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy Otto, Edgar A; Ramaswami, Gokul; Janssen, Sabine; Chaki, Moumita; ... Hildebrandt, Friedhelm 2011
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Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease Lesage, S; Condroyer, C; Lannuzel, A; Lohmann, E; ... Brice, A 2009
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Recurrent inactivation of the PRDM1 gene in primary central nervous system lymphoma Courts, Cornelius; Montesinos-Rongen, Manuel; Brunn, Anna; Bug, Stefanie; ... Deckert, Martina 2008
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Molecular analysis of F8 in Lebanese haemophilia A patients: novel mutations and phenotype-genotype correlation Djambas Khayat, C.; Salem, N.; Chouery, E.; Corbani, S.; ... Mégarbané, A. 2008
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Identification of low frequency knockout mutants in Dictyostelium discoideum created by single or double homologous recombination Charette, Steve; Cornillon, Sophie Marie; Cosson, Pierre 2006
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Severe factor XI deficiency in a Lebanese family: identification of a novel missense mutation (Trp501Cys) in the catalytic domain De Moerloose, Philippe; Germanos-Haddad, Myrna; Boehlen, Françoise; Neerman Arbez, Marguerite 2004