176 related articles for article (PubMed ID: 10422811)
1. High frequency of de novo deletions in Mexican Duchenne and Becker muscular dystrophy patients. Implications for genetic counseling.
Alcántara MA; Villarreal MT; Del Castillo V; Gutiérrez G; Saldaña Y; Maulen I; Lee R; Macías M; Orozco L
Clin Genet; 1999 May; 55(5):376-80. PubMed ID: 10422811
[TBL] [Abstract][Full Text] [Related]
2. Carrier diagnosis of Duchenne muscular dystrophy using restriction fragment length polymorphisms.
Hejtmancik JF; Harris SG; Tsao CC; Ward PA; Caskey CT
Neurology; 1986 Dec; 36(12):1553-62. PubMed ID: 2878392
[TBL] [Abstract][Full Text] [Related]
3. Use of serum creatine kinase, pyruvate kinase, and genetic linkage for carrier detection in Duchenne and Becker dystrophy.
Hyser CL; Griggs RC; Mendell JR; Polakowska R; Quirk S; Brooke MH; Fenichel GM; Doherty RA
Neurology; 1987 Jan; 37(1):4-10. PubMed ID: 2879259
[TBL] [Abstract][Full Text] [Related]
4. Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.
Lindlöf M; Kääriäinen H; Davies KE; de la Chapelle A
J Med Genet; 1986 Dec; 23(6):560-72. PubMed ID: 2879928
[TBL] [Abstract][Full Text] [Related]
5. Detection of Duchenne and Becker muscular dystrophy carriers by quantitative multiplex polymerase chain reaction analysis.
Ioannou P; Christopoulos G; Panayides K; Kleanthous M; Middleton L
Neurology; 1992 Sep; 42(9):1783-90. PubMed ID: 1513470
[TBL] [Abstract][Full Text] [Related]
6. Molecular probe protocol for determining carrier status in Duchenne and Becker muscular dystrophies.
Prior TW; Friedman KJ; Highsmith WE; Perry TR; Silverman LM
Clin Chem; 1990 Mar; 36(3):441-5. PubMed ID: 1968788
[TBL] [Abstract][Full Text] [Related]
7. Carrier detection and microsatellite analysis of Duchenne and Becker muscular dystrophy in Spanish families.
Kruyer H; Miranda M; Volpini V; Estivill X
Prenat Diagn; 1994 Feb; 14(2):123-30. PubMed ID: 7910399
[TBL] [Abstract][Full Text] [Related]
8. Direct carrier detection by in situ suppression hybridization with cosmid clones of the Duchenne/Becker muscular dystrophy locus.
Ried T; Mahler V; Vogt P; Blonden L; van Ommen GJ; Cremer T; Cremer M
Hum Genet; 1990 Oct; 85(6):581-6. PubMed ID: 2227948
[TBL] [Abstract][Full Text] [Related]
9. Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial results.
Kääriäinen H; Lindlöf M; Somer H; de la Chapelle A
Clin Genet; 1990 Mar; 37(3):179-87. PubMed ID: 1969777
[TBL] [Abstract][Full Text] [Related]
10. Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy.
Hodgson SV; Bobrow M
Br Med Bull; 1989 Jul; 45(3):719-44. PubMed ID: 2688825
[TBL] [Abstract][Full Text] [Related]
11. Determination of carrier status in Duchenne and Becker muscular dystrophies by quantitative polymerase chain reaction and allele-specific oligonucleotides.
Prior TW; Papp AC; Snyder PJ; Highsmith WE; Friedman KJ; Perry TR; Silverman LM; Mendell JR
Clin Chem; 1990 Dec; 36(12):2113-7. PubMed ID: 2253356
[TBL] [Abstract][Full Text] [Related]
12. Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy.
Schwartz LS; Tarleton J; Popovich B; Seltzer WK; Hoffman EP
Am J Hum Genet; 1992 Oct; 51(4):721-9. PubMed ID: 1415217
[TBL] [Abstract][Full Text] [Related]
13. Molecular deletion analysis in Duchenne muscular dystrophy.
Thomas NS; Ray PN; Worton RG; Harper PS
J Med Genet; 1986 Dec; 23(6):509-15. PubMed ID: 2879923
[TBL] [Abstract][Full Text] [Related]
14. Rapid direct diagnosis of deletions carriers of Duchenne and Becker muscular dystrophies.
Fassati A; Tedeschi S; Bordoni A; Amboni P; Curcio C; Bresolin N; Scarlato G
Lancet; 1994 Jul; 344(8918):302-3. PubMed ID: 7914263
[TBL] [Abstract][Full Text] [Related]
15. The value of deletion analysis for carrier detection in Duchenne muscular dystrophy (DMD).
Bejjani B; Finn P; Milunsky A; Amos J
Clin Genet; 1991 Apr; 39(4):245-52. PubMed ID: 2070545
[TBL] [Abstract][Full Text] [Related]
16. Analysis of dystrophin gene deletions in patients from the Mexican population with Duchenne/Becker muscular dystrophy.
Coral-Vázquez R; Arenas D; Cisneros B; Peñaloza L; Kofman S; Salamanca F; Montañez C
Arch Med Res; 1993; 24(1):1-6. PubMed ID: 8292871
[TBL] [Abstract][Full Text] [Related]
17. Carrier detection in Duchenne and Becker muscular dystrophy Argentine families.
Baranzini SE; Giliberto F; Dalamon V; Barreiro C; García-Erro M; Grippo J; Szijan I
Clin Genet; 1998 Dec; 54(6):503-11. PubMed ID: 9894797
[TBL] [Abstract][Full Text] [Related]
18. Carrier detection in Becker muscular dystrophy using creatine kinase estimation and DNA analysis.
Kingston HM; Sarfarazi M; Newcombe RG; Willis N; Harper PS
Clin Genet; 1985 Apr; 27(4):383-91. PubMed ID: 3995787
[TBL] [Abstract][Full Text] [Related]
19. The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy.
Hodgson S; Walker A; Cole C; Hart K; Johnson L; Heckmatt J; Dubowitz V; Bobrow M
J Med Genet; 1987 Mar; 24(3):152-9. PubMed ID: 3572997
[TBL] [Abstract][Full Text] [Related]
20. Carrier detection of Duchenne/Becker muscular dystrophy by using fluorescent linkage analysis in Taiwan.
Lee CC; Wu MC; Wu JY; Li TC; Tsai FJ; Tsai CH
Acta Paediatr Taiwan; 2000; 41(2):69-74. PubMed ID: 10927942
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]