Mutations of the Flavin-Containing Monooxygenase Gene (FMO3) cause Trimethylaminuria, a Defect in Detoxication von Treacy, E. P., Akerman, B. R., Chow, L. M. L., Youil, R., Lin, C. Bibeau, J., Bruce, A. G., Knight, M., Danks, D. M., Cashman, J. R., Forrest, S. M.

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Dramatically Different Phenotypes in Mouse Models of Human Tay-Sachs and Sandhoff Diseases von Phaneuf, Daniel, Wakamatsu, Nobuaki, Huang, Jing-Qi, Borowski, Anita, Peterson, Alan C., Fortunato, Sheila R., Ritter, Gerd, Igdoura, Suleiman A., Morales, Carlos R., Benoit, Guylaine, Akerman, Beverly R., Leclerc, Daniel, Hanai, Nobuo, Marth, Jamey D., Trasler, Jacquetta M., Gravel, Roy A.

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A View from America: Map Collecting, 'Treasure-House' Libraries, and American Civic Influences on the History of Cartography von Akerman, James R.

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Kenneth Nebenzahl (16 September 1927-29 January 2020) von Karrow, Robert W., Akerman, Jr. James R.

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In Vivo Variability of TMA Oxidation Is Partially Mediated by Polymorphisms of the FMO3 Gene von Lambert, Deborah M., Mamer, Orval A., Akerman, Beverley R., Choinière, Luc, Gaudet, Daniel, Hamet, Pavel, Treacy, Eileen P.

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Postoperative Echolalia and Catatonia Responsive to Gamma Aminobutyric Acid Receptor Agonists in a Liver Transplant Patient von Seetharam, Pragyna, Akerman, Riva R.

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Trimethylaminuria Is Caused by Mutations of the FMO3 Gene in a North American Cohort von Akerman, B.R., Lemass, H., Chow, L.M.L., Lambert, D.M., Greenberg, C., Bibeau, C., Mamer, O.A., Treacy, E.P.

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Reflections on the birth of conjoined twins von Poole, Richard F

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Characterization of Phenylketonuria Missense Substitutions, Distant from the Phenylalanine Hydroxylase Active Site, Illustrates a Paradigm for Mechanism and Potential Modulation of... von Waters, Paula J., Parniak, Michael A., Akerman, Beverly R., Scriver, Charles R.

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Missense mutations in the phenylalanine hydroxylase gene (PAH) can cause accelerated proteolytic turnover of PAH enzyme: A mechanism underlying phenylketonuria von Waters, P. J., Parniak, M. A., Akerman, B. R., Jones, A. O., Scriver, C. R.

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Two novel mutations of the FMO3 gene in a proband with trimethylaminuria von Akerman, B.R., Forrest, S., Chow, L., Youil, R., Knight, M., Treacy, E.P.

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Sequence of DNA flanking the exons of the HEXA gene, and identification of mutations in Tay-Sachs disease von TRIGGS-RAINE, B. L, AKERMAN, B. R, CLARKE, J. T. R, GRAVAL, R. A

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Mutations participating in interallelic complementation in propionic acidemia von GRAVEL, R. A, AKERMAN, B. R, LAMHONWAH, A.-M, LOYER, M, LEON-DEL-RIO, A, ITALIANO, I

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Mapping, Battlefield Guidebooks, and Remembering the Great War von Akerman, James R.

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American Promotional Road Mapping in the Twentieth Century von Akerman, James R.

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Novel mutations and DNA-based screening in non-Jewish carriers of Tay-Sachs disease von AKERMAN, B. R, NATOWICZ, M. R, KABACK, M. M, LOYER, M, CAMPEAU, E, GRAVEL, R. A

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The structuring of political territory in early printed atlases von Akerman, James R.

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A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screening von Triggs-Raine, B L, Mules, E H, Kaback, M M, Lim-Steele, J S, Dowling, C E, Akerman, B R, Natowicz, M R, Grebner, E E, Navon, R, Welch, J P

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Reflections on the birth of conjoined twins von Akerman, Beverly R.

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A second, large deletion in the HEXB gene in a patient with infantile Sandhoff disease von Zhang, Zhi-Xin, Wakamatsu, Nobuaki, Akerman, Beverly R., Mules, Emily H., Thomas, George H., Gravel, Roy A.

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