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Search Results - Sémonin, Olivier
Search Results - Sémonin, Olivier
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A Rare Case of a Patient Heterozygous for the Hemochromatosis Mutation C282Y and Homozygous for H63D
by
Lucotte, Gérard
,
Champenois, Thierry
,
Sémonin, Olivier
Published in
Blood cells, molecules, & diseases
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A de novo heterozygous deletion of 42 base-pairs in the noggin gene of a fibrodysplasia ossificans progressiva patient
by
Lucotte, G
,
Sémonin, O
,
Lutz, P
Published in
Clinical genetics
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Identification of three novel mutations of the noggin gene in patients with fibrodysplasia ossificans progressiva
by
Sémonin, Olivier
,
Fontaine, Karine
,
Daviaud, Christian
,
Ayuso, Carmen
,
Lucotte, Gérard
Published in
American journal of medical genetics
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A de novo heterozygous deletion of 42 base-pairs in the noggin gene of a fibrodysplasia ossificansprogressiva patient
by
Lucotte, Gérard
,
Sémonin, Olivier
,
Lutz, Patrick
Published in
Clinical genetics
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Both upstream and intragenic sequences of the human neurofilament light gene direct expression of lacZ in neurons of transgenic mouse embryos
by
Leconte, L
,
Semonin, O
,
Zvara, A
,
Boisseau, S
,
Poujeol, C
,
Julien, J P
,
Simonneau, M
Published in
Journal of molecular neuroscience
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Both upstream and intragenic sequences of the human neurofilament light gene direct expression oflacZ in neurons of transgenic mouse embryos
by
Leconte, Laurence
,
Semonin, Olivier
,
Zvara, Agnès
,
Boisseau, Sylvie
,
Poujeol, Chantal
,
Julien, Jean-Pierre
,
Simonneau, Michel
Published in
Journal of molecular neuroscience
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