Trichoepithelioma is a benign cutaneous tumour that originates from hair follicles and occurs either as a sporadic non-familial or a multiple-familial type. Recently, several mutations in the cylindromatosis (CYLD) gene have been reported in multiple familial trichoepithelioma (MFT)
Familial cylindromatosis is an autosomal dominant predisposition to multiple neoplasms of the skin a...
Aim-The gene for familial cylindromatosis (CYLD) has been localised to chromosome 16q, and has recen...
Brooke-Spiegler syndrome (BSS) is a rare, inherited, autosomal dominant disorder characterized by de...
Multiple familial trichoepithelioma (MFT) is an autosomal dominant skin disease characterized by the...
The clinical presentation of multiple, rare, skin appendage tumours called cylindromas has been attr...
Brooke–Spiegler syndrome (BSS, familial cylindromatosis or turban tumor syndrome) is an inherited di...
Mutations in the tumor suppressor gene CYLD underlie phenotypically heterogeneous hereditary tumor d...
Mutations in the tumor suppressor gene CYLD underlie phenotypically heterogeneous hereditary tumor d...
Cylindromas are benign appendage tumors mainly found on the scalp, but they can occur on any hair-be...
Brooke–Spiegler syndrome (BSS), familial cylindromatosis (FC), and multiple familial trichoepithelio...
Germ-line mutations in CYLD are found in patients with familial skin appendage tumours. The protein ...
Familial cylindromatosis (turban tumor syndrome; Brooke–Spiegler syndrome) (OMIM numbers 123850, 132...
Familial cylindromatosis is an autosomal dominant genetic predisposition to multiple tumours of the ...
textabstractPathogenic mutations in CYLD can be identified in patients affected with Brooke-Spiegler...
Hereditary cylindromatosis is a rare autosomal dominant disease characterised by the development of ...
Familial cylindromatosis is an autosomal dominant predisposition to multiple neoplasms of the skin a...
Aim-The gene for familial cylindromatosis (CYLD) has been localised to chromosome 16q, and has recen...
Brooke-Spiegler syndrome (BSS) is a rare, inherited, autosomal dominant disorder characterized by de...
Multiple familial trichoepithelioma (MFT) is an autosomal dominant skin disease characterized by the...
The clinical presentation of multiple, rare, skin appendage tumours called cylindromas has been attr...
Brooke–Spiegler syndrome (BSS, familial cylindromatosis or turban tumor syndrome) is an inherited di...
Mutations in the tumor suppressor gene CYLD underlie phenotypically heterogeneous hereditary tumor d...
Mutations in the tumor suppressor gene CYLD underlie phenotypically heterogeneous hereditary tumor d...
Cylindromas are benign appendage tumors mainly found on the scalp, but they can occur on any hair-be...
Brooke–Spiegler syndrome (BSS), familial cylindromatosis (FC), and multiple familial trichoepithelio...
Germ-line mutations in CYLD are found in patients with familial skin appendage tumours. The protein ...
Familial cylindromatosis (turban tumor syndrome; Brooke–Spiegler syndrome) (OMIM numbers 123850, 132...
Familial cylindromatosis is an autosomal dominant genetic predisposition to multiple tumours of the ...
textabstractPathogenic mutations in CYLD can be identified in patients affected with Brooke-Spiegler...
Hereditary cylindromatosis is a rare autosomal dominant disease characterised by the development of ...
Familial cylindromatosis is an autosomal dominant predisposition to multiple neoplasms of the skin a...
Aim-The gene for familial cylindromatosis (CYLD) has been localised to chromosome 16q, and has recen...
Brooke-Spiegler syndrome (BSS) is a rare, inherited, autosomal dominant disorder characterized by de...