Results
|
33941.
|
Reduced expression of hMSH2 protein is correlated to poor survival for soft tissue sarcoma patients. [electronic resource] by
- Taubert, Helge W
- Bartel, Frank
- Kappler, Matthias
- Schuster, Katja
- Meye, Axel
- Lautenschläger, Christine
- Thamm-Mücke, Barbara
- Bache, Matthias
- Schmidt, Hannelore
- Holzhausen, Hans-Jürgen
- Würl, Peter
Producer: 20030520
In:
Cancer vol. 97
Availability: No items available.
|
|
33942.
|
|
|
33943.
|
|
|
33944.
|
|
|
33945.
|
|
|
33946.
|
Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1. [electronic resource] by
- Young, T L
- Ives, E
- Lynch, E
- Person, R
- Snook, S
- MacLaren, L
- Cater, T
- Griffin, A
- Fernandez, B
- Lee, M K
- King, M C
- Cator, T
Producer: 20020221
In:
Human molecular genetics vol. 10
Availability: No items available.
|
|
33947.
|
Complete genomic screen in Parkinson disease: evidence for multiple genes. [electronic resource] by
- Scott, W K
- Nance, M A
- Watts, R L
- Hubble, J P
- Koller, W C
- Lyons, K
- Pahwa, R
- Stern, M B
- Colcher, A
- Hiner, B C
- Jankovic, J
- Ondo, W G
- Allen, F H
- Goetz, C G
- Small, G W
- Masterman, D
- Mastaglia, F
- Laing, N G
- Stajich, J M
- Slotterbeck, B
- Booze, M W
- Ribble, R C
- Rampersaud, E
- West, S G
- Gibson, R A
- Middleton, L T
- Roses, A D
- Haines, J L
- Scott, B L
- Vance, J M
- Pericak-Vance, M A
Producer: 20011228
In:
JAMA vol. 286
Availability: No items available.
|
|
33948.
|
|
|
33949.
|
Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors. [electronic resource] by
- Bahuau, M
- Vidaud, D
- Jenkins, R B
- Bièche, I
- Kimmel, D W
- Assouline, B
- Smith, J S
- Alderete, B
- Cayuela, J M
- Harpey, J P
- Caille, B
- Vidaud, M
Producer: 19980707
In:
Cancer research vol. 58
Availability: No items available.
|
|
33950.
|
|
|
33951.
|
|
|
33952.
|
ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia. [electronic resource] by
- Cavé, H
- Cacheux, V
- Raynaud, S
- Brunie, G
- Bakkus, M
- Cochaux, P
- Preudhomme, C
- Laï, J L
- Vilmer, E
- Grandchamp, B
Producer: 19971016
In:
Leukemia vol. 11
Availability: No items available.
|
|
33953.
|
|
|
33954.
|
|
|
33955.
|
|
|
33956.
|
|
|
33957.
|
|
|
33958.
|
Ten novel MSH2 and MLH1 germline mutations in families with HNPCC. [electronic resource] by
- Krüger, Stefan
- Bier, Andrea
- Plaschke, Jens
- Höhl, Ruth
- Aust, Daniela E
- Kreuz, Friedmar R
- Pistorius, Steffen R
- Saeger, Hans D
- Rothhammer, Veit
- Al-Taie, Oliver
- Schackert, Hans K
Producer: 20050331
In:
Human mutation vol. 24
Availability: No items available.
|
|
33959.
|
|
|
33960.
|
Chromosome 17p13.2 transfer reverts transformation phenotypes and Fas-mediated apoptosis in breast epithelial cells. [electronic resource] by
- Lareef, Mohamed H
- Tahin, Quivo
- Song, Joon
- Russo, Irma H
- Mihaila, Dana
- Slater, Carolyn M
- Balsara, Binaifer
- Testa, Joseph R
- Broccoli, Dominique
- Grobelny, Jennifer V
- Mor, Gil
- Cuthbert, Andrew
- Russo, Jose
Producer: 20040430
In:
Molecular carcinogenesis vol. 39
Availability: No items available.
|