160 related articles for article (PubMed ID: 3777020)
1. 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]
2. 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]
3. 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]
4. 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]
5. In utero fetal muscle biopsy for the diagnosis of Duchenne muscular dystrophy in a female fetus "suddenly at risk".
Evans MI; Farrell SA; Greb A; Ray P; Johnson MP; Hoffman EP
Am J Med Genet; 1993 May; 46(3):309-12. PubMed ID: 8488877
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. 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]
10. Duchenne muscular dystrophy in a girl with a 45,X/46,XX/47,XXX chromosome constitution.
Bortolini ER; da Silva DM; Chequer RS; Vianna-Morgante AM; Zatz M
Am J Med Genet; 1986 Oct; 25(2):239-43. PubMed ID: 3777022
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. An X:autosome translocation stabilizes truncated dystrophin: implications for lack of truncated dystrophins in Duchenne muscular dystrophy.
Fidzianska A; Morrone A; Pegoraro E; Ryniewicz B; Ilnicka A; Zammarchi E; Hoffman EP
Neuropediatrics; 1995 Jun; 26(3):163-7. PubMed ID: 7477755
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. 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]
15. X inactivation and dystrophin studies in a t(X;12) female: evidence for biochemical normalization in Duchenne muscular dystrophy carriers.
Wenger SL; Steele MW; Hoffman EP; Barmada MA; Wessel HB
Am J Med Genet; 1992 Aug; 43(6):1012-5. PubMed ID: 1415326
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
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. Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndrome.
Ellison KA; Roth EJ; McCabe ER; Chinault AC; Zoghbi HY
Am J Med Genet; 1993 Nov; 47(7):1124-34. PubMed ID: 8291533
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
