Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: a clinically and genetically distinct syndrome
Jackson, C E, Norum, R A, Boyd, S B, Talpos, G B, Wilson, S D, Taggart, R T, Mallette, L E
Published in Surgery (01.12.1990)
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Published in Surgery (01.12.1990)
Journal Article
Adrenoleukodystrophy: Evidence for X Linkage, Inactivation, and Selection Favoring the Mutant Allele in Heterozygous Cells
Migeon, Barbara R., Moser, Hugo W., Moser, Ann B., Axelman, Joyce, Sillence, David, Norum, Robert A.
Published in Proceedings of the National Academy of Sciences - PNAS (01.08.1981)
Published in Proceedings of the National Academy of Sciences - PNAS (01.08.1981)
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Journal Article
Characterization of apoA- and apoB-containing lipoprotein particles in a variant of familial apoA-I deficiency with planar xanthoma: the metabolic significance of LP-A-II particles
Bekaert, ED, Alaupovic, P, Knight-Gibson, CS, Laux, MJ, Pelachyk, JM, Norum, RA
Published in Journal of lipid research (01.10.1991)
Published in Journal of lipid research (01.10.1991)
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Journal Article
Clinical value of tumor doubling estimations in multiple endocrine neoplasia type II
Jackson, C E, Talpos, G B, Block, M A, Norum, R A, Lloyd, R V, Tashjian, Jr, A H
Published in Surgery (01.12.1984)
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Published in Surgery (01.12.1984)
Journal Article
Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2
Gardner, E, Papi, L, Easton, D F, Cummings, T, Jackson, C E, Kaplan, M, Love, D R, Mole, S E, Moore, J K, Mulligan, L M
Published in Human molecular genetics (01.03.1993)
Published in Human molecular genetics (01.03.1993)
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Journal Article
Linkage of the multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2A
Norum, Robert A., Lafreniere, Ronald G., O'Neal, Lawrence W., Nikolai, Thomas F., Delaney, J.P., Sisson, James C., Sobol, Hagay, Lenoir, Gilbert M., Ponder, Bruce A.J., Willard, Huntington F., Jackson, Charles E.
Published in Genomics (San Diego, Calif.) (01.10.1990)
Published in Genomics (San Diego, Calif.) (01.10.1990)
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Journal Article
BRCA1 maps proximal to D17S579 on chromosome 17q21 by genetic analysis
Chamberlain, J S, Boehnke, M, Frank, T S, Kiousis, S, Xu, J, Guo, S W, Hauser, E R, Norum, R A, Helmbold, E A, Markel, D S
Published in American journal of human genetics (01.04.1993)
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Published in American journal of human genetics (01.04.1993)
Journal Article
Familial apolipoprotein AI and apolipoprotein CIII deficiency. Subclass distribution, composition, and morphology of lipoproteins in a disorder associated with premature atherosclerosis
Forte, T M, Nichols, A V, Krauss, R M, Norum, R A
Published in The Journal of clinical investigation (01.11.1984)
Published in The Journal of clinical investigation (01.11.1984)
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Journal Article
alpha-1-antitrypsin and disease
Norum, R A, Bearn, A G, Briscoe, W A, Briscoe, A
Published in The Mount Sinai journal of medicine (01.11.1977)
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Published in The Mount Sinai journal of medicine (01.11.1977)
Journal Article
Familial Deficiency of Apolipoproteins A-I and C-III and Precocious Coronary-Artery Disease
Norum, Robert A, Lakier, Jeffrey B, Goldstein, Sidney, Angel, Aubie, Goldberg, Ronald B, Block, Walter D, Noffze, Donna K, Dolphin, Peter J, Edelglass, John, Bogorad, David D, Alaupovic, Petar
Published in The New England journal of medicine (24.06.1982)
Published in The New England journal of medicine (24.06.1982)
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Journal Article