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Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1-related disorders.
Published in:
Clinical Genetics, 2015, v. 87, n. 5, p. 430, doi. 10.1111/cge.12437
By:
- Chaussenot, A.;
- Rouzier, C.;
- Quere, M.;
- Plutino, M.;
- Ait‐El‐Mkadem, S.;
- Bannwarth, S.;
- Barth, M.;
- Dollfus, H.;
- Charles, P.;
- Nicolino, M.;
- Chabrol, B.;
- Vialettes, B.;
- Paquis‐Flucklinger, V.
Publication type:
Article
A novel homozygous MMP2 mutation in a family with Winchester syndrome.
Published in:
Clinical Genetics, 2006, v. 69, n. 3, p. 271, doi. 10.1111/j.1399-0004.2006.00584.x
By:
- Rouzier, C.;
- Vanatka, R.;
- Bannwarth, S.;
- Philip, N.;
- Coussement, A.;
- Paquis-Flucklinger, V.;
- Lambert, J.-C.
Publication type:
Article
Ex vivo expansion of CD34+/CD41+ late progenitors from enriched peripheral blood CD34+ cells.
Published in:
2000
By:
- Halle, P.;
- Rouzier, C.;
- Kanold, J.;
- Boiret, N.;
- Rapatel, C.;
- Mareynat, G.;
- Tchirkov, A.;
- Berger, M.;
- Travade, P.;
- Bonhomme, J.;
- Deméocq, F.;
- Deméocq, F
Publication type:
journal article
The Frequency of Germline BRCA and Non-BRCA HR-Gene-Variants in a Cohort of Pancreatic Cancer Patients.
Published in:
Digestive Diseases & Sciences, 2023, v. 68, n. 4, p. 1525, doi. 10.1007/s10620-022-07733-z
By:
- Baz, M.;
- Gondran-Teiller, V.;
- Bressac, B.;
- Cabaret, O.;
- Fievet, A.;
- Dimaria, M.;
- Goldbarg, V.;
- Colas, C.;
- Bonnet-Dupeyron, M. N.;
- Tinat, J.;
- Lebrun, M.;
- Mari, V.;
- Limacher, J. M.;
- Corsini, C.;
- Ginglinger, E.;
- Saurin, J. C.;
- Brahimi, A.;
- Rouzier, C.;
- Giraud, S.;
- Schuster, H.
Publication type:
Article

Found: 4

Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1-related disorders.

A novel homozygous MMP2 mutation in a family with Winchester syndrome.

Ex vivo expansion of CD34+/CD41+ late progenitors from enriched peripheral blood CD34+ cells.

The Frequency of Germline BRCA and Non-BRCA HR-Gene-Variants in a Cohort of Pancreatic Cancer Patients.