Conrad, Bernard

 
 
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2012

Scientific Articles

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Clinical, functional and genetic analysis of twenty-four patients with chronic granulomatous disease - identification of eight novel mutations in CYBB and NCF2 genesMartel, Cécile; Mollin, Michelle; Conrad, Bernard; Posfay Barbe, Klara;

2008

Scientific Articles

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Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypesMefford, H. C.; Gimelli, Stefania; Conrad, Bernard; Antonarakis, Stylianos;

2007

Scientific Articles

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Gene duplication: a drive for phenotypic diversity and cause of human diseaseConrad, Bernard; Antonarakis, Stylianos;
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Sequence variation in ultraconserved and highly conserved elements does not cause X-linked mental retardationBottani, Armand; Chelly, Jamel; de Brouwer, A. P.; Pardo, Bruno; ... Conrad, Bernard
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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 FGD1Bottani, Armand; Orrico, Alfredo; Galli, Lucia; Karam, Oliver Laurent; ... Conrad, Bernard

2005

Scientific Articles

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Transcriptional activation by bidirectional RNA polymerase II elongation over a silent promoterLeupin, Olivier; Attanasio, Catia; Marguerat, Samuel; Tapernoux, Myriam; ... Conrad, Bernard

1998

Scientific Articles

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A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patientsMasternak, Krzysztof; Barras, Emmanuele; Zufferey, Madeleine; Conrad, Bernard; ... Reith, Walter
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