Works by Lepretre F

Results: 7

Dissection of an inverted X(p21.3q27.1) chromosome associated with mental retardation.

Published in:

Cytogenetic & Genome Research, 2003, v. 101, n. 2, p. 124, doi. 10.1159/000074167

By:

Leprêtre, F.;
Delannoy, V.;
Froguel, P.;
Vasseur, F.;
Montepellier, C.

Publication type:

Article

Mutation screening and association studies of the human uncoupling protein 3 gene in normoglycemic and diabetic morbidly obese patients.

Published in:

1999

By:

Otabe, Shuichi;
Clement, Karine;
Dubois, Severine;
Lepretre, Frederic;
Pelloux, Veronique;
Leibel, Rudolph;
Chung, Wendy;
Boutin, Philippe;
Guy-Grand, Bernard;
Froguel, Philippe;
Vasseur, Francis;
Otabe, S;
Clement, K;
Dubois, S;
Lepretre, F;
Pelloux, V;
Leibel, R;
Chung, W;
Boutin, P;
Guy-Grand, B

Publication type:

journal article

Monitoring of the microstructure of ion-irradiated nuclear ceramics by in situ Raman spectroscopy.

Published in:

Journal of Raman Spectroscopy, 2016, v. 47, n. 4, p. 476, doi. 10.1002/jrs.4837

By:

Miro, S.;
Bordas, E.;
Thomé, L.;
Costantini, J.‐M.;
Leprêtre, F.;
Trocellier, P.;
Serruys, Y.;
Beck, L.;
Gosset, D.;
Verlet, R.;
Huguet‐Garcia, J.;
Tupin, M.;
Belleil, M.

Publication type:

Article

A synonymous coding polymorphism in the alpha2-Heremans-schmid glycoprotein gene is associated with type 2 diabetes in French Caucasians.

Published in:

2005

By:

Siddiq A;
Lepretre F;
Hercberg S;
Froguel P;
Gibson F;
Siddiq, Afshan;
Lepretre, Frederic;
Hercberg, Serge;
Froguel, Philippe;
Gibson, Fernando

Publication type:

journal article

Commissioning of the Iseult CEA 11.7 T whole-body MRI: current status, gradient–magnet interaction tests and first imaging experience.

Published in:

MAGMA: Magnetic Resonance Materials in Physics, Biology & Medicine, 2023, v. 36, n. 2, p. 175, doi. 10.1007/s10334-023-01063-5

By:

Boulant, Nicolas;
Quettier, Lionel;
Aubert, G.;
Amadon, A.;
Belorgey, J.;
Berriaud, C.;
Bonnelye, C.;
Bredy, Ph.;
Chazel, E.;
Dilasser, G.;
Dubois, O.;
Giacomini, E.;
Gilgrass, G.;
Gras, V.;
Guihard, Q.;
Jannot, V.;
Juster, F. P.;
Lannou, H.;
Leprêtre, F.;
Lerman, C.

Publication type:

Article

Molecular and cytogenetic characterisation of a small interstitial de novo 20p13→p12.3 deletion in a patient with severe growth deficit.

Published in:

Cytogenetics & Cell Genetics, 2001, v. 94, n. 3/4, p. 142, doi. 10.1159/000048806

By:

Leprêtre, F.;
Montpellier, A C.;
Delannoy, V.;
Froguel, P.;
Vasseur, F.

Publication type:

Article

Waved aCGH: to smooth or not to smooth.

Published in:

Nucleic Acids Research, 2010, v. 38, n. 7, p. e94

By:

Leprêtre, F.;
Villenet, C.;
Quief, S.;
Nibourel, O.;
Jacquemin, C.;
Troussard, X.;
Jardin, F.;
Gibson, F.;
Kerckaert, J. P.;
Roumier, C.;
Figeac, M.

Publication type:

Article