APA

Kovach M. J., Waggoner B., Leal S. M., Gelber D., Khardori R., Levenstien M. A., Shanks C. A., Gregg G., Al-Lozi M. T., Miller T., Rakowicz W., Lopate G., Florence J., Glosser G., Simmons Z., Morris J. C., Whyte M. P., Pestronk A. & Kimonis V. E. (20020313). 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 dementia. : Molecular genetics and metabolism.

Chicago

Kovach M J, Waggoner B, Leal S M, Gelber D, Khardori R, Levenstien M A, Shanks C A, Gregg G, Al-Lozi M T, Miller T, Rakowicz W, Lopate G, Florence J, Glosser G, Simmons Z, Morris J C, Whyte M P, Pestronk A and Kimonis V E. 20020313. 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 dementia. : Molecular genetics and metabolism.

Harvard

Kovach M. J., Waggoner B., Leal S. M., Gelber D., Khardori R., Levenstien M. A., Shanks C. A., Gregg G., Al-Lozi M. T., Miller T., Rakowicz W., Lopate G., Florence J., Glosser G., Simmons Z., Morris J. C., Whyte M. P., Pestronk A. and Kimonis V. E. (20020313). 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 dementia. : Molecular genetics and metabolism.

MLA

Kovach M J, Waggoner B, Leal S M, Gelber D, Khardori R, Levenstien M A, Shanks C A, Gregg G, Al-Lozi M T, Miller T, Rakowicz W, Lopate G, Florence J, Glosser G, Simmons Z, Morris J C, Whyte M P, Pestronk A and Kimonis V E. 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 dementia. : Molecular genetics and metabolism. 20020313.