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. 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) ↗