136 related articles for article (PubMed ID: 6123008)
1. X chromosome in Duchenne muscular dystrophy.
Spowart G; Buckton KE; Skinner R; Emery AE
Lancet; 1982 May; 1(8283):1251. PubMed ID: 6123008
[No Abstract] [Full Text] [Related]
2. An (X;11) translocation in a girl with Duchenne muscular dystrophy. Repository identification No. GM1695.
Greenstein RM; Reardon MP; Chan TS; Middleton AB; Mulivor RA; Greene AE; Coriell LL
Cytogenet Cell Genet; 1980; 27(4):268. PubMed ID: 7438786
[No Abstract] [Full Text] [Related]
3. [A combination of Duchenne's progressive muscular dystrophy with congenital ichthyosis--a deletion or 2 independent gene mutations at Xp21--Xp22?].
Badalian LO; Temin PA; Kamennykh LN; Zavadenko NN; Arkhipov BA
Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(8):48-51. PubMed ID: 3195282
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. [Restriction polymorphism of 3 human genomic probes on the short arm of the X chromosome in a reference population, and applications in prenatal and carrier female diagnosis of Duchenne's muscular dystrophy].
Dandieu S; Guérin P; Lucotte G
C R Acad Sci III; 1985; 301(6):271-6. PubMed ID: 3928103
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Echinocytes in families with Duchenne muscular dystrophy.
Soltan HC
J Med Genet; 1977 Aug; 14(4):276-8. PubMed ID: 926140
[TBL] [Abstract][Full Text] [Related]
12. Carrier detection and gene analysis of Duchenne muscular dystrophy.
Pearson PL; van Ommen GJ; Bakker E
Cold Spring Harb Symp Quant Biol; 1986; 51 Pt 1():353-8. PubMed ID: 2884063
[No Abstract] [Full Text] [Related]
13. Molecular genetics of Duchenne and Becker muscular dystrophy.
Worton RG; Burghes AH
Int Rev Neurobiol; 1988; 29():1-76. PubMed ID: 3042661
[No Abstract] [Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. [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]
18. 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]
19. 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]
20. [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]
[Next] [New Search]
