These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. Human ornithine transcarbamylase locus mapped to band Xp21.1 near the Duchenne muscular dystrophy locus. Lindgren V; de Martinville B; Horwich AL; Rosenberg LE; Francke U Science; 1984 Nov; 226(4675):698-700. PubMed ID: 6494904 [TBL] [Abstract][Full Text] [Related]
3. Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation. Ingle C; Williamson R; de la Chapelle A; Herva RR; Haapala K; Bates G; Willard HF; Pearson P; Davies KE Am J Hum Genet; 1985 May; 37(3):451-62. PubMed ID: 2988331 [TBL] [Abstract][Full Text] [Related]
4. Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome. Francke U; Ochs HD; de Martinville B; Giacalone J; Lindgren V; Distèche C; Pagon RA; Hofker MH; van Ommen GJ; Pearson PL Am J Hum Genet; 1985 Mar; 37(2):250-67. PubMed ID: 4039107 [TBL] [Abstract][Full Text] [Related]
5. Regional localisation of X chromosome short arm probes. Paulsen K; Forrest S; Scherer G; Ropers HH; Davies K Hum Genet; 1986 Oct; 74(2):155-9. PubMed ID: 3464558 [TBL] [Abstract][Full Text] [Related]
6. Mapping of 12 translocation breakpoints in the Xp21 region with respect to the locus for Duchenne muscular dystrophy. Boyd Y; Cockburn D; Holt S; Munro E; Van Ommen GJ; Gillard B; Affara N; Ferguson-Smith M; Craig I Cytogenet Cell Genet; 1988; 48(1):28-34. PubMed ID: 3180845 [TBL] [Abstract][Full Text] [Related]
7. Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families. Dorkins H; Junien C; Mandel JL; Wrogemann K; Moison JP; Martinez M; Old JM; Bundey S; Schwartz M; Carpenter N Hum Genet; 1985; 71(2):103-7. PubMed ID: 2995231 [TBL] [Abstract][Full Text] [Related]
8. Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome. Davies KE; Pearson PL; Harper PS; Murray JM; O'Brien T; Sarfarazi M; Williamson R Nucleic Acids Res; 1983 Apr; 11(8):2303-12. PubMed ID: 6304647 [TBL] [Abstract][Full Text] [Related]
9. Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy. Hofker MH; Wapenaar MC; Goor N; Bakker E; van Ommen GJ; Pearson PL Hum Genet; 1985; 70(2):148-56. PubMed ID: 2989153 [TBL] [Abstract][Full Text] [Related]
11. DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21. Greenberg CR; Hamerton JL; Nigli M; Wrogemann K Am J Hum Genet; 1987 Aug; 41(2):128-37. PubMed ID: 3475976 [TBL] [Abstract][Full Text] [Related]
12. Human X chromosome markers and Duchenne muscular dystrophy. Davies KE; Speer A; Herrmann F; Spiegler AW; McGlade S; Hofker MH; Briand P; Hanke R; Schwartz M; Steinbicker V Nucleic Acids Res; 1985 May; 13(10):3419-26. PubMed ID: 3859837 [TBL] [Abstract][Full Text] [Related]
13. Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosome. Brown CS; Pearson PL; Thomas NS; Sarfarazi M; Harper PS; Shaw DJ J Med Genet; 1985 Jun; 22(3):179-81. PubMed ID: 2989525 [TBL] [Abstract][Full Text] [Related]
14. Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids. Roncuzzi L; Fadda S; Mochi M; Prosperi L; Sangiorgi S; Santamaria R; Sbarra D; Besana D; Morandi L; Rocchi M Am J Hum Genet; 1985 Mar; 37(2):407-17. PubMed ID: 2984927 [TBL] [Abstract][Full Text] [Related]
15. Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy. Brown CS; Thomas NS; Sarfarazi M; Davies KE; Kunkel L; Pearson PL; Kingston HM; Shaw DJ; Harper PS Hum Genet; 1985; 71(1):62-74. PubMed ID: 2993158 [TBL] [Abstract][Full Text] [Related]
16. De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy. Chelly J; Marlhens F; Le Marec B; Jeanpierre M; Lambert M; Hamard G; Dutrillaux B; Kaplan JC Hum Genet; 1986 Oct; 74(2):193-6. PubMed ID: 2876949 [TBL] [Abstract][Full Text] [Related]
18. Muscular dystrophy in girls with X;autosome translocations. Boyd Y; Buckle V; Holt S; Munro E; Hunter D; Craig I J Med Genet; 1986 Dec; 23(6):484-90. PubMed ID: 3806636 [TBL] [Abstract][Full Text] [Related]
19. Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21. Jacobs PA; Hunt PA; Mayer M; Bart RD Am J Hum Genet; 1981 Jul; 33(4):513-8. PubMed ID: 7258185 [TBL] [Abstract][Full Text] [Related]
20. Construction of a human X-chromosome-enriched phage library which facilitates analysis of specific loci. Kunkel LM; Lalande M; Monaco AP; Flint A; Middlesworth W; Latt SA Gene; 1985; 33(3):251-8. PubMed ID: 2989089 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]