Malignant connective tissue tumors, particularly soft-tissue sarcomas and os-teosarcomas, are recognized complica-tions of hereditary retinoblastoma (1,2). An apparent high frequency of lipomas, which are benign tumors of adipose tis-sue, among survivors of retinoblastoma was noted by a patient with hereditary retinoblastoma attending a recent meet-ing of the New England Retinoblastoma Family Support Group. Because we knew of no published reports of an as-sociation between germline mutations in the retinoblastoma (RB1) gene and lipo-mas, we examined data from a cohort of 898 retinoblastoma survivors, diagnosed at several New York hospitals durin
Retinoblastoma is a rare cancer of the infant retina that is diagnosed in approximately 8,000 childr...
Retinoblastoma represents the prototypic model for inherited cancers. The RB1 gene was the first tum...
International audienceRetinoblastoma (Rb) results from biallelic inactivation of the RB1 gene. Hered...
Patients who have survived heredi-tary retinoblastoma are at increased risk of dying of a sarcoma, a...
Hereditary retinoblastoma survivors have substantially increased risk of subsequent malignant neopla...
Item does not contain fulltextSurvivors of hereditary retinoblastoma have a high risk of second prim...
BACKGROUND:Retinoblastoma is the most common malignant ocular tumour of childhood. It results from m...
Retinoblastoma is a rare malignant tumor that arises in the retina. Patients with a positive family ...
Survivors of hereditary retinoblastoma have a high risk of second primary malignancies, but it has n...
Retinoblastoma is the most common intraocular malignant tumor in childhood. Approximately 45% of ret...
Constitutional mutations in the RB1 gene predispose to retinoblastoma development. Hence genetic scr...
Hereditary retinoblastoma is attributed to germline mutation in an RB1 tumor suppressor gene followe...
International audienceBackground: Retinoblastoma (Rb) is a rare intraocular malignant tumor in child...
The nature of the tumorigenic mutation was analyzed in 30 retinoblastoma (Rb) tumors (16 non-heredit...
Retinoblastoma is a pediatric tumor which is associated with somatic and inherited mutations at the ...
Retinoblastoma is a rare cancer of the infant retina that is diagnosed in approximately 8,000 childr...
Retinoblastoma represents the prototypic model for inherited cancers. The RB1 gene was the first tum...
International audienceRetinoblastoma (Rb) results from biallelic inactivation of the RB1 gene. Hered...
Patients who have survived heredi-tary retinoblastoma are at increased risk of dying of a sarcoma, a...
Hereditary retinoblastoma survivors have substantially increased risk of subsequent malignant neopla...
Item does not contain fulltextSurvivors of hereditary retinoblastoma have a high risk of second prim...
BACKGROUND:Retinoblastoma is the most common malignant ocular tumour of childhood. It results from m...
Retinoblastoma is a rare malignant tumor that arises in the retina. Patients with a positive family ...
Survivors of hereditary retinoblastoma have a high risk of second primary malignancies, but it has n...
Retinoblastoma is the most common intraocular malignant tumor in childhood. Approximately 45% of ret...
Constitutional mutations in the RB1 gene predispose to retinoblastoma development. Hence genetic scr...
Hereditary retinoblastoma is attributed to germline mutation in an RB1 tumor suppressor gene followe...
International audienceBackground: Retinoblastoma (Rb) is a rare intraocular malignant tumor in child...
The nature of the tumorigenic mutation was analyzed in 30 retinoblastoma (Rb) tumors (16 non-heredit...
Retinoblastoma is a pediatric tumor which is associated with somatic and inherited mutations at the ...
Retinoblastoma is a rare cancer of the infant retina that is diagnosed in approximately 8,000 childr...
Retinoblastoma represents the prototypic model for inherited cancers. The RB1 gene was the first tum...
International audienceRetinoblastoma (Rb) results from biallelic inactivation of the RB1 gene. Hered...