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Search Results - Oudet, Claudine L.
Search Results - Oudet, Claudine L.
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MEPE, a New Gene Expressed in Bone Marrow and Tumors Causing Osteomalacia
by
Rowe, Peter S.N
,
de Zoysa, Priyal A
,
Dong, Rong
,
Wang, Huei Rong
,
White, Kenneth E
,
Econs, Michael J
,
Oudet, Claudine L
Published in
Genomics (San Diego, Calif.)
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Distribution of Mutations in the PEX Gene in Families with X-linked Hypophosphataemic Rickets (HYP)
by
Rowe, Peter S. N.
,
Oudet, Claudine L.
,
Francis, Fiona
,
Sinding, Christiane
,
Pannetier, Solange
,
Econs, Mike J.
,
Strom, Tim M.
,
Meitinger, Thomas
,
Garabedian, Michele
,
David, Albert
,
Macher, Marie-Alice
,
Questiaux, Elisabeth
,
Popowska, Ewa
,
Pronicka, Ewa
,
Read, Andrew P.
,
Mokrzycki, Agnes
,
Glorieux, Francis H.
,
Drezner, Marc K.
,
Hanauer, Andre
,
Lehrach, Hans
,
Goulding, Johnathan N.
,
O'Riordan, Jeffrey L. H.
Published in
Human molecular genetics
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Unterkieferpropulsion durch eine im Oberkiefer fixierte Vorbißführung mit seitlicher Bißsperre von unterschiedlicher Höhe hinsichtlich der täglichen Dauer der Behandlung
by
Petrovic, Alexandre G.
,
Oudet, Claudine L.
,
Shaye, Robert
Published in
Fortschritte der Kieferorthopädie
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Frequent genomic abnormalities at TWIST in human pediatric osteosarcomas
by
Entz‐Werlé, Natacha
,
Stoetzel, Corinne
,
Berard‐Marec, Perrine
,
Kalifa, Chantal
,
Brugiere, Laurence
,
Pacquement, Hélène
,
Schmitt, Claudine
,
Tabone, Marie‐Dominique
,
Gentet, Jean‐Claude
,
Quillet, Robert
,
Oudet, Pierre
,
Lutz, Patrick
,
Babin‐Boilletot, Annie
,
Gaub, Marie‐Pierre
,
Perrin‐Schmitt, Fabienne
Published in
International journal of cancer
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Involvement of MET/TWIST/APC Combination or the Potential Role of Ossification Factors in Pediatric High-Grade Osteosarcoma Oncogenesis
by
Entz-Werle, Natacha
,
Lavaux, Thomas
,
Metzger, Nadia
,
Stoetzel, Corinne
,
Lasthaus, Christelle
,
Marec, Perrine
,
Kalita, Chantal
,
Brugieres, Laurence
,
Pacquement, Helene
,
Schmitt, Claudine
,
Tabone, Marie-Dominique
,
Gentet, Jean-Claude
,
Lutz, Patrick
,
Babin, Annie
,
Oudet, Pierre
,
Gaub, Marie Pierre
,
Perrin-Schmitt, Fabienne
Published in
Neoplasia (New York, N.Y.)
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Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets
by
Francis, F
,
Strom, T M
,
Hennig, S
,
Böddrich, A
,
Lorenz, B
,
Brandau, O
,
Mohnike, K L
,
Cagnoli, M
,
Steffens, C
,
Klages, S
,
Borzym, K
,
Pohl, T
,
Oudet, C
,
Econs, M J
,
Rowe, P S
,
Reinhardt, R
,
Meitinger, T
,
Lehrach, H
Published in
Genome research
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M13 endopeptidases: New conserved motifs correlated with structure, and simultaneous phylogenetic occurrence of PHEX and the bony fish
by
Bianchetti, Laurent
,
Oudet, Claudine
,
Poch, Olivier
Published in
Proteins, structure, function, and bioinformatics
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Functional Implications of the Spectrum of Mutations Found in 234 Cases With X-linked Juvenile Retinoschisis (XLRS)
by
The Retinoschisis Consortium
Published in
Human molecular genetics
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Two hot spots of recombination in the DMD gene correlate with the deletion prone regions
by
Oudet, Claudine
,
Hanauer, André
,
Clemens, Paula
,
Caskey, Thomas
,
Mandel, Jean-Louis
Published in
Human molecular genetics
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Nonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombination
by
Oudet, C
,
Heilig, R
,
Hanauer, A
,
Mandel, J L
Published in
American journal of human genetics
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New markers for linkage analysis of X-linked hypophosphataemic rickets
by
ROWE, P. S. N
,
GOULDING, J
,
O'RIORDAN, J. L. H
,
READ, A
,
MOUNTFORD, R
,
HANAUER, A
,
OUDET, C
,
WHYTE, M. P
,
MEIER-EWERT, S
,
LEHRACH, H
,
DAVIES, K. E
Published in
Human genetics
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Human Molecular Genetics
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Diseases Of The Osteoarticular System
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Hypophosphatemia, Familial - Genetics
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