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British Journal of Cancer|October 17, 2003
ATM variants 7271T>G and IVS10-6T>G among women with unilateral and bilateral breast cancerJ L Bernstein, L Bernstein, W D Thompson, et al.
Molecular Genetics and Metabolism|December 26, 2001
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementiaM J Kovach, B Waggoner, S M Leal, et al.
The Journal of Clinical Endocrinology and Metabolism|November 26, 2010
Alendronate for the treatment of pediatric osteogenesis imperfecta: a randomized placebo-controlled studyL M Ward, F Rauch, M P Whyte, et al.
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