Results
|
321.
|
|
|
322.
|
Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident. [electronic resource] by
- Wicking, C
- Shanley, S
- Smyth, I
- Gillies, S
- Negus, K
- Graham, S
- Suthers, G
- Haites, N
- Edwards, M
- Wainwright, B
- Chenevix-Trench, G
Producer: 19970123
In:
American journal of human genetics vol. 60
Availability: No items available.
|
|
323.
|
|
|
324.
|
|
|
325.
|
|
|
326.
|
|
|
327.
|
|
|
328.
|
|
|
329.
|
|
|
330.
|
Severe PATCHED1 Deficiency in Cancer-Prone Gorlin Patient Cells Results in Intrinsic Radiosensitivity. [electronic resource] by
- Vulin, Adeline
- Sedkaoui, Melissa
- Moratille, Sandra
- Sevenet, Nicolas
- Soularue, Pascal
- Rigaud, Odile
- Guibbal, Laure
- Dulong, Joshua
- Jeggo, Penny
- Deleuze, Jean-François
- Lamartine, Jérôme
- Martin, Michèle T
Producer: 20190109
In:
International journal of radiation oncology, biology, physics vol. 102
Availability: No items available.
|
|
331.
|
|
|
332.
|
Prenatal manifestation in a family affected by nevoid basal cell carcinoma syndrome. [electronic resource] by
- Le Brun Keris, Yann
- Jouk, Pierre-Simon
- Saada-Sebag, Géraldine
- Roux, Jean-Jacques
- Mattei, Bertrand
- Bagait, Laure
- Paoloni-Giacobino, Ariane
- Grandchamp, Bernard
- Soufir, Nadem
- Lespinasse, James
Producer: 20081113
In:
European journal of medical genetics vol. 51
Availability: No items available.
|
|
333.
|
|
|
334.
|
|
|
335.
|
|
|
336.
|
|
|
337.
|
|
|
338.
|
|
|
339.
|
|
|
340.
|
|