152 related articles for article (PubMed ID: 1670611)
1. The diagnosis of Duchenne and Becker muscular dystrophies: two years' experience in a comprehensive carrier screening and prenatal diagnostic laboratory.
Laing NG; Mears ME; Chandler DC; Layton MG; Thomas HE; Johnsen RD; Goldblatt J; Kakulas BA
Med J Aust; 1991 Jan; 154(1):14-8. PubMed ID: 1670611
[TBL] [Abstract][Full Text] [Related]
2. Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.
Sugino S; Fujishita S; Kamimura N; Matsumoto T; Wapenaar MC; Deng HX; Shibuya N; Miike T; Niikawa N
Am J Med Genet; 1989 Dec; 34(4):555-61. PubMed ID: 2576185
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Molecular biological approaches to genetic disorders in prenatal diagnosis.
Katayama S
Early Hum Dev; 1992; 29(1-3):149-53. PubMed ID: 1356752
[TBL] [Abstract][Full Text] [Related]
5. Possibilities and limitation of prenatal diagnosis and carrier determination for Duchenne and Becker muscular dystrophy using cDNA probes.
Speer A; Spiegler AW; Hanke R; Grade K; Giertler U; Schieck J; Forrest S; Davies KE; Neumann R; Bollmann R
J Med Genet; 1989 Jan; 26(1):1-5. PubMed ID: 2918522
[TBL] [Abstract][Full Text] [Related]
6. Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA.
Darras BT; Koenig M; Kunkel LM; Francke U
Am J Med Genet; 1988 Mar; 29(3):713-26. PubMed ID: 2897793
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy by restriction fragment length polymorphism analysis with pERT 87 deoxyribonucleic acid probes.
Katayama S; Montano M; Slotnick RN; Lebo RV; Golbus MS
Am J Obstet Gynecol; 1988 Mar; 158(3 Pt 1):548-55. PubMed ID: 2894769
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.
Bakker E; Bonten EJ; De Lange LF; Veenema H; Majoor-Krakauer D; Hofker MH; Van Ommen GJ; Pearson PL
J Med Genet; 1986 Dec; 23(6):573-80. PubMed ID: 2879929
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis and carrier detection by DNA studies in a Duchenne muscular dystrophy family with no living affected male.
Chen JD; Denton MJ; Serravalle S; Morgan G
Aust Paediatr J; 1988 Dec; 24(6):351-3. PubMed ID: 2907402
[TBL] [Abstract][Full Text] [Related]
11. Deletion screening and prenatal diagnosis of Duchenne muscular dystrophy using cDNA probes Cf 23a and Cf 56a.
Herrmann FH; Wulff K; Schütz M; Wehnert M
Eur J Pediatr; 1990 Jan; 149(4):263-5. PubMed ID: 1968008
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis in a female carrying a deletion close to the Duchenne locus.
Børresen AL; Boman H; Møller P; Berg K
Prenat Diagn; 1988 Jan; 8(1):67-72. PubMed ID: 3422736
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of Duchenne muscular dystrophy by DNA analysis.
Old JM; Davies KE
J Med Genet; 1986 Dec; 23(6):556-9. PubMed ID: 2879927
[TBL] [Abstract][Full Text] [Related]
14. Distinction of Becker from limb-girdle muscular dystrophy by means of dystrophin cDNA probes.
Norman A; Thomas N; Coakley J; Harper P
Lancet; 1989 Mar; 1(8636):466-8. PubMed ID: 2563842
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis using deletion studies in Duchenne muscular dystrophy.
Speer MC; Pericak-Vance MA; Yamaoka LH; Koh J; Hung WY; Gaskell PC; Vance JM; Bartlett RJ; Roses AD
Prenat Diagn; 1988 Jul; 8(6):427-37. PubMed ID: 3211845
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis of Duchenne muscular dystrophy: prospective linkage analysis and retrospective dystrophin cDNA analysis.
Ward PA; Hejtmancik JF; Witkowski JA; Baumbach LL; Gunnell S; Speer J; Hawley P; Tantravahi U; Caskey CT
Am J Hum Genet; 1989 Feb; 44(2):270-81. PubMed ID: 2643315
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNA.
Upadhyaya M; Smith RA; Thomas NS; Norman AM; Harper PS
Clin Genet; 1990 Jun; 37(6):456-62. PubMed ID: 2200624
[TBL] [Abstract][Full Text] [Related]
19. DNA polymorphisms and deletion analysis of the Duchenne-Becker muscular dystrophy gene in the Chinese.
Soong BW; Tsai TF; Su CH; Kao KP; Hsiao KJ; Su TS
Am J Med Genet; 1991 Mar; 38(4):593-600. PubMed ID: 1676564
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
