Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer.
Uterine leiomyomata (fibroids) are common and clinically important tumors, but little is known about their etiology and pathogenesis. We previously mapped a gene that predisposes to multiple fibroids, cutaneous leiomyomata and renal cell carcinoma to chromosome 1q42.3-q43 (refs 4-6). Here we show, t...
Prif Awduron: | Tomlinson, I, Alam, N, Rowan, A, Barclay, E, Jaeger, E, Kelsell, D, Leigh, I, Gorman, P, Lamlum, H, Rahman, S, Roylance, R, Olpin, S, Bevan, S, Barker, K, Hearle, N, Houlston, R, Kiuru, M, Lehtonen, R, Karhu, A, Vilkki, S, Laiho, P, Eklund, C, Vierimaa, O, Aittomäki, K, Hietala, M |
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Fformat: | Journal article |
Iaith: | English |
Cyhoeddwyd: |
2002
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Eitemau Tebyg
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Localisation of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43
gan: Alam, A, et al.
Cyhoeddwyd: (2001) -
Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43
gan: Alam, N, et al.
Cyhoeddwyd: (2001) -
Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43.
gan: Alam, N, et al.
Cyhoeddwyd: (2001)