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A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients Masternak, Krzysztof; Barras, Emmanuele; Zufferey, Madeleine; Conrad, Bernard; ... Reith, Walter 1998
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Gene duplication: a drive for phenotypic diversity and cause of human disease Conrad, Bernard; Antonarakis, Stylianos 2007
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Sequence variation in ultraconserved and highly conserved elements does not cause X-linked mental retardation Bottani, Armand; Chelly, Jamel; de Brouwer, A. P.; Pardo, Bruno; ... Conrad, Bernard 2007
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Transcriptional activation by bidirectional RNA polymerase II elongation over a silent promoter Leupin, Olivier; Attanasio, Catia; Marguerat, Samuel; Tapernoux, Myriam; ... Conrad, Bernard 2005
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Unilateral focal polymicrogyria in a patient with classical Aarskog-Scott syndrome due to a novel missense mutation in an evolutionary conserved RhoGEF domain of the faciogenital dysplasia gene FGD1 Bottani, Armand; Orrico, Alfredo; Galli, Lucia; Karam, Oliver Laurent; ... Conrad, Bernard 2007