Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43
Alam NA, Bevan S, Churchman M et al. Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43. Am J Hum Genet 2001; 68: 1264-9.
Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathology
Kiuru M, Launonen V, Hietala M et al. Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathology. Am J Pathol 2001; 159: 825-9.
Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency
Alam NA, Rowan AJ, Wortham NC et al. Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency. Hum Mol Genet 2003; 12: 1241-52.
Germline fumarate hydratase mutations in families with multiple cutaneous and uterine leiomyomata
Martinez-Mir A, Glaser B, Chuang G et al. Germline fumarate hydratase mutations in families with multiple cutaneous and uterine leiomyomata. J Invest Dermatol 2003; 121: 741-4.
Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer
Tomlinson IP, Alam NA, Rowan AJ et al. Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer. Nat Genet 2002; 30: 406-10.
Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in north America
Toro JR, Nickerson ML, Wei M-H et al. Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in north America. Am J Hum Genet 2003; 73: 95-106.
Few FH mutations in sporadic counterparts of tumor types observed in hereditary leiomyomatosis and renal cell cancer families
Kiuru M, Lehtonen R, Arola J et al. Few FH mutations in sporadic counterparts of tumor types observed in hereditary leiomyomatosis and renal cell cancer families. Cancer Res 2002; 62: 4554-7.
Low frequency of somatic mutations in the FH/multiple cutaneous leiomyomatosis gene in sporadic leiomyosarcomas and uterine leiomyomas
Barker KT, Bevan S, Wang R et al. Low frequency of somatic mutations in the FH/multiple cutaneous leiomyomatosis gene in sporadic leiomyosarcomas and uterine leiomyomas. Br J Cancer 2002; 87: 446-8.
Biallelic inactivation of fumarate hydatase (FH) occurs in the non-syndromic uterine leiomyomas but is rare in other tumors
Lehtonen R, Kiuru M, Vanharanta S et al. Biallelic inactivation of fumarate hydatase (FH) occurs in the non-syndromic uterine leiomyomas but is rare in other tumors. Am J Pathol 2004; 164: 17-22.