1. Novel mutation in the PTCH1 gene in a patient with Gorlin syndrome with prominent clinical features. (1st April 2014) Authors: Valdivielso‐Ramos, M.; Solera, J.; Mauleon, C.; Hernanz, J. M.; Amiñoso, C.; Galiano, S.; De la Cueva, P. Journal: Clinical and experimental dermatology Issue: Volume 39:Number 3(2014) Page Start: 406 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Novel mutation in the PTCH1 gene in a patient with Gorlin syndrome with prominent clinical features. (April 2014) Authors: Valdivielso‐Ramos, M.; Solera, J.; Mauleon, C.; Hernanz, J. M.; Amiñoso, C.; Galiano, S.; De, P. Journal: Clinical and experimental dermatology Issue: Volume 39:Number 3(2014) Page Start: 406 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. PanGen-Fam: Spanish registry of hereditary pancreatic cancer. Issue 14 (September 2015) Authors: Mocci, E.; Guillen-Ponce, C.; Earl, J.; Marquez, M.; Solera, J.; Salazar-López, M.-T.; Calcedo-Arnáiz, C.; Vázquez-Sequeiros, E.; Montans, J.; Muñoz-Beltrán, M.; Vicente-Bártulos, A.; González-Gordaliza, C.; Sanjuanbenito, A.; Guerrero, C.; Mendía, E.; Lisa, E.; Lobo, E.; Martínez, J.C.; Real, F.... Journal: European journal of cancer Issue: Volume 51:Issue 14(2015:Sep.) Page Start: 1911 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. PanGen-Fam: Spanish registry of hereditary pancreatic cancer. Issue 14 (September 2015) Authors: Mocci, E.; Guillen-Ponce, C.; Earl, J.; Marquez, M.; Solera, J.; Salazar-López, M.-T.; Calcedo-Arnáiz, C.; Vázquez-Sequeiros, E.; Montans, J.; Muñoz-Beltrán, M.; Vicente-Bártulos, A.; González-Gordaliza, C.; Sanjuanbenito, A.; Guerrero, C.; Mendía, E.; Lisa, E.; Lobo, E.; Martínez, J.C.; Real, F.... Journal: European journal of cancer Issue: Volume 51:Issue 14(2015:Sep.) Page Start: 1911 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Recurrence of Hirschsprung disease due to maternal mosaicism of a novel RET gene mutation. (13th May 2013) Authors: Amiñoso, C.; García‐Miñaúr, S.; Martínez, L.; Tenorio, J.A.; Tovar, J.A.; Lapunzina, P.; Solera, J. Journal: Clinical genetics Issue: Volume 85:Number 4(2014:Apr.) Page Start: 401 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗