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Un cas rare de myélome multiple non-sécrétant.
Published in:
Annales de Biologie Clinique, 2022, v. 80, n. 1, p. 61, doi. 10.1684/abc.2022.1699
By:
- Bintner, Tristan;
- Coulon, Valérie;
- Cabrera, Quentin;
- Klein, Thierry
Publication type:
Article
Allelic imbalance, including deletion of PTEN/MMAC1, at the Cowden disease locus on 10q22-23, in hamartomas from patients with cowden syndrome and germline PTEN mutation.
Published in:
Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 61, doi. 10.1002/(SICI)1098-2264(199801)21:1<61::AID-GCC8>3.0.CO;2-6
By:
- Marsh, Debbie J.;
- Dahia, Patricia L. M.;
- Coulon, Valérie;
- Zheng, Zimu;
- Dorion-Bonnet, Françoise;
- Call, Katherine M.;
- Little, Randall;
- Lin, Albert Y.;
- Eeles, Rosalind A.;
- Goldstein, Alisa M.;
- Hodgson, Shirley V.;
- Richardson, Anne-Louise;
- Robinson, Bruce G.;
- Weber, H. Christian;
- Longy, Michel;
- Eng, Charis
Publication type:
Article
Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation.
Published in:
Human Molecular Genetics, 1998, v. 7, n. 3, p. 507, doi. 10.1093/hmg/7.3.507
By:
- Marsh, Debbie J.;
- Coulon, Valérie;
- Lunetta, Kathryn L.;
- Rocca‐Serra, Philippe;
- Dahia, Patricia L. M.;
- Zheng, Zimu;
- Liaw, Danny;
- Caron, Stacey;
- Duboué, Bernadette;
- Lin, Albert Y.;
- Richardson, Anne‐Louise;
- Bonnetblanc, Jean‐Marie;
- Bressieux, Jean‐Marie;
- Cabarrot‐Moreau, Agnés;
- Chompret, Agnés;
- Demange, Liliane;
- Eeles, Rosalind A.;
- Yahanda, Alan M.;
- Fearon, Eric R.;
- Fricker, Jean-Pierre
Publication type:
Article

Found: 3

Un cas rare de myélome multiple non-sécrétant.

Allelic imbalance, including deletion of PTEN/MMAC1, at the Cowden disease locus on 10q22-23, in hamartomas from patients with cowden syndrome and germline PTEN mutation.

Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation.