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Conrad, Bernard
Conrad, Bernard
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Elements: 7
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2012
Scientific Articles
unige:31691
Clinical, functional and genetic analysis of twenty-four patients with chronic granulomatous disease - identification of eight novel mutations in CYBB and NCF2 genes
Martel, Cécile; Mollin, Michelle;
Conrad, Bernard
;
Posfay Barbe, Klara
;
2008
Scientific Articles
unige:9219
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes
Mefford, H. C.;
Gimelli, Stefania
;
Conrad, Bernard
;
Antonarakis, Stylianos
;
2007
Scientific Articles
unige:9159
Gene duplication: a drive for phenotypic diversity and cause of human disease
Conrad, Bernard
;
Antonarakis, Stylianos
;
unige:8654
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
unige:43113
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
2005
Scientific Articles
unige:8856
Transcriptional activation by bidirectional RNA polymerase II elongation over a silent promoter
Leupin, Olivier;
Attanasio, Catia
;
Marguerat, Samuel
;
Tapernoux, Myriam
; ...
Conrad, Bernard
1998
Scientific Articles
unige:11446
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
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