Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng849z.pdf
Reference17 articles.
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2. Luoto, R. et al. Heritability and risk factors of uterine fibroids—the Finnish Twin Cohort study. Maturitas 37, 15–26 (2000).
3. Takamizawa, S. et al. Risk of complications and uterine malignancies in women undergoing hysterectomy for presumed benign leiomyomas. Gynecol. Obstet. Invest. 48, 193–196 (1999).
4. Alam, N.A. et al. Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3–q43. Am. J. Hum. Genet. 68, 1264–1269 (2001).
5. Kiuru, M. et al. Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathology. Am. J. Pathol. 159, 825–829 (2001).
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