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Page 1
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
Kunkel LM, Hejtmancik JF, Caskey CT, Speer A, Monaco AP, Middlesworth W, Colletti CA, Bertelson C, Müller U, Bresnan M, Shapiro F, Tantravahi U, Speer J, Latt SA, Bartlett R, Pericak-Vance MA, Roses AD, Thompson MW, Ray PN, Worton RG, Fischbeck KH, Gallano P, Coulon M, Duros C, Boue J, Junien C, Chelly J, Hamard G, Jeanpierre M, Lambert M, Kaplan JC, Emery A, Dorkins H, McGlade S, Davies KE, Boehm C, Arveiler B, Lemaire C, Morgan GJ, Denton MJ, Amos J, Bobrow M, Benham F, Boswinkel E, Cole C, Dubowitz V, Hart K, Hodgson S, Johnson L, Walker A, Roncuzzi L, Ferlini A, Nobile C, Romeo G, Wilcox DE, Affara NA, Ferguson-Smith MA, Lindolf M, Kaariainen H, de la Chapelle A, Ionasescu V, Searby C, Ionasescu R, Bakker E, van Ommen GJ, Pearson PL, Greenberg CR, Hamerton JL, Wrogemann K, Doherty RA, Polakowska R, Hyser C, Quirk S, Thomas N, Harper JF, Darras BT, Francke U. Kunkel LM, et al. Among authors: emery a. Nature. 1986 Jul 3-9;322(6074):73-7. doi: 10.1038/322073a0. Nature. 1986. PMID: 3014348
Antenatal diagnosis of Duchenne muscular dystrophy.
Emery AE, Burt D, Dubowitz V, Rocker I, Donnai D, Harris R, Donnai P. Emery AE, et al. Lancet. 1979 Apr 21;1(8121):847-9. doi: 10.1016/s0140-6736(79)91264-9. Lancet. 1979. PMID: 86094
Erythrocyte spectrin in Duchenne muscular dystrophy.
Anand R, Emery AE. Anand R, et al. Among authors: emery ae. Clin Chim Acta. 1981 Dec 24;117(3):345-54. doi: 10.1016/0009-8981(81)90122-4. Clin Chim Acta. 1981. PMID: 7318186
Linkage between the loci for benign (Becker-type) X-borne muscular dystrophy and deutan colour blindness.
Skinner R, Smith C, Emery AE. Skinner R, et al. Among authors: emery ae. J Med Genet. 1974 Dec;11(4):317-20. doi: 10.1136/jmg.11.4.317. J Med Genet. 1974. PMID: 4548442 Free PMC article.
A family is described in which benign Becker type X-linked muscular dystrophy and deutan colour blindness are segregating. The lod scores from this family have been added to those obtained in a family previously reported (Emery et.al, 1968/1969) and give an e
A family is described in which benign Becker type X-linked muscular dystrophy and deutan colour blindness are segregating. The lod sc
474 results