196 related articles for article (PubMed ID: 6745920)
1. Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome.
Verellen-Dumoulin C; Freund M; De Meyer R; Laterre C; Frédéric J; Thompson MW; Markovic VD; Worton RG
Hum Genet; 1984; 67(1):115-9. PubMed ID: 6745920
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
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. Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy.
Boyd Y; Buckle VJ
Clin Genet; 1986 Feb; 29(2):108-15. PubMed ID: 3955860
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Duchenne muscular dystrophy in a girl with chromosomal translocation].
Werneck LC; Lemos SM; Magdalena N
Arq Neuropsiquiatr; 1988 Dec; 46(4):401-5. PubMed ID: 3245772
[TBL] [Abstract][Full Text] [Related]
17. Characterisation, phenotypic manifestations and X-inactivation pattern in 14 patients with X-autosome translocations.
Kalz-Füller B; Sleegers E; Schwanitz G; Schubert R
Clin Genet; 1999 May; 55(5):362-6. PubMed ID: 10422808
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypes.
Disteche CM; Swisshelm K; Forbes S; Pagon RA
Hum Genet; 1984; 66(1):71-6. PubMed ID: 6698557
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]