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.
83 related articles for article (PubMed ID: 3279979)
1. [Duchenne muscular dystrophy (DMD) in a female with an X-autosome translocation]. Uchida T; Ogata H; Shirai Z; Mitsudome A No To Hattatsu; 1988 Jan; 20(1):28-32. PubMed ID: 3279979 [No Abstract] [Full Text] [Related]
2. 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]
3. Clinical features in a girl with Duchenne muscular dystrophy with an X-autosome translocation; (X;4)(p21;q26). Kimura S; Mitsuda T; Misugi N; Saito F; Tonomura A; Sugita H Brain Dev; 1986; 8(6):619-23. PubMed ID: 3826553 [TBL] [Abstract][Full Text] [Related]
4. Further evidence for Xp21 location of Duchenne muscular dystrophy (DMD) locus: X;9 translocation in a female with DMD. Emanuel BS; Zackai EH; Tucker SH J Med Genet; 1983 Dec; 20(6):461-3. PubMed ID: 6655672 [TBL] [Abstract][Full Text] [Related]
5. Duchenne muscular dystrophy in a female with a translocation involving Xp21. Nevin NC; Hughes AE; Calwell M; Lim JH J Med Genet; 1986 Apr; 23(2):171-3. PubMed ID: 3712394 [TBL] [Abstract][Full Text] [Related]
6. Duchenne muscular dystrophy in a girl with an (X;15) translocation. Ribeiro MC; Melaragno MI; Schmidt B; Brunoni D; Gabbai AA; Hackel C Am J Med Genet; 1986 Oct; 25(2):231-6. PubMed ID: 3777020 [TBL] [Abstract][Full Text] [Related]
7. Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophy. Bodrug SE; Ray PN; Gonzalez IL; Schmickel RD; Sylvester JE; Worton RG Science; 1987 Sep; 237(4822):1620-4. PubMed ID: 3629260 [TBL] [Abstract][Full Text] [Related]
8. [Duchenne muscular dystrophy in a female with an X-autosome translocation]. Narazaki O; Hanai T; Ueki Y; Mitsudome A Rinsho Shinkeigaku; 1985 Apr; 25(4):432-6. PubMed ID: 4017373 [No Abstract] [Full Text] [Related]
9. 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]
10. Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus. Zatz M; Vianna-Morgante AM; Campos P; Diament AJ J Med Genet; 1981 Dec; 18(6):442-7. PubMed ID: 7334502 [TBL] [Abstract][Full Text] [Related]
11. Mapping of four translocation breakpoints within the Duchenne muscular dystrophy gene. Bodrug SE; Burghes AH; Ray PM; Worton RG Genomics; 1989 Jan; 4(1):101-4. PubMed ID: 2914705 [TBL] [Abstract][Full Text] [Related]
12. X;autosome translocations in females with Duchenne or Becker muscular dystrophy. Dubowitz V Nature; 1986 Jul 17-23; 322(6076):291-2. PubMed ID: 3461282 [No Abstract] [Full Text] [Related]
13. Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm. Lindenbaum RH; Clarke G; Patel C; Moncrieff M; Hughes JT J Med Genet; 1979 Oct; 16(5):389-92. PubMed ID: 513085 [TBL] [Abstract][Full Text] [Related]
14. Xp21/autosome translocations. Case report and risk for Duchenne muscular dystrophy. Holden JJ; Smith A; MacLeod PM; Masotti R; Duncan AM Clin Genet; 1986 Jun; 29(6):516-22. PubMed ID: 3742857 [TBL] [Abstract][Full Text] [Related]
15. The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27 beta methylation analysis. Robinson DO; Boyd Y; Cockburn D; Collinson MN; Craig I; Jacobs PA Genet Res; 1990; 56(2-3):135-40. PubMed ID: 2272503 [TBL] [Abstract][Full Text] [Related]
16. Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy. Bodrug SE; Roberson JR; Weiss L; Ray PN; Worton RG; Van Dyke DL J Med Genet; 1990 Jul; 27(7):426-32. PubMed ID: 2395160 [TBL] [Abstract][Full Text] [Related]
17. Turner's syndrome and Duchenne muscular dystrophy in a girl with an X; autosome translocation. Bjerglund Nielsen L; Nielsen IM Ann Genet; 1984; 27(3):173-7. PubMed ID: 6334482 [TBL] [Abstract][Full Text] [Related]
18. High-resolution banding study of an X/4 translocation in a female with Duchenne muscular dystrophy. Saito F; Tonomura A; Kimura S; Misugi N; Sugita H Hum Genet; 1985; 71(4):370-1. PubMed ID: 4077054 [TBL] [Abstract][Full Text] [Related]
19. Prenatal evaluation of a de novo X;9 translocation. Feldman B; Kramer RL; Ebrahim SA; Wolff DJ; Evans MI Am J Med Genet; 1999 Aug; 85(5):476-8. PubMed ID: 10405445 [TBL] [Abstract][Full Text] [Related]
20. Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy. Kean VM; Macleod HL; Thompson MW; Ray PN; Verellen-Dumoulin C; Worton RG J Med Genet; 1986 Dec; 23(6):491-3. PubMed ID: 2879921 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]