181 related articles for article (PubMed ID: 1451547)
1. Potential pitfalls in using DNA probes to counsel Duchenne and Becker muscular dystrophy families.
Shi YJ; Fischbeck KH; Ritter A
Chin Med J (Engl); 1992 Jun; 105(6):469-75. PubMed ID: 1451547
[TBL] [Abstract][Full Text] [Related]
2. Experience with DNA analysis in Duchenne and Becker muscular dystrophy families in NSW.
Morgan G; Donald JA; Chen J; Serravalle S; Colley P; Denton MJ
Aust Paediatr J; 1988; 24 Suppl 1():98-9. PubMed ID: 3202741
[TBL] [Abstract][Full Text] [Related]
3. Case of the month: germline mosaicism in carriers of Duchenne muscular dystrophy.
Prior TW; Papp AC; Snyder PJ; Mendell JR
Muscle Nerve; 1992 Aug; 15(8):960-3. PubMed ID: 1353862
[TBL] [Abstract][Full Text] [Related]
4. Application of DNA probes to carrier detection and prenatal diagnosis of Duchenne (and Becker) muscular dystrophy.
Mulley JC; Gedeon AK; Haan EA; Sheffield LJ; White SJ; Bates LJ; Robertson EF; Sutherland GR
Aust Paediatr J; 1988; 24 Suppl 1():92-7. PubMed ID: 3202740
[TBL] [Abstract][Full Text] [Related]
5. Carrier detection and prenatal diagnosis of Duchenne/Becker muscular dystrophy (D/BMD) by DNA-analysis.
Bakker E; Bonten EJ; den Dunnen JT; Veenema H; Grootscholten PM; van Ommen GJ; Pearson PL
Prog Clin Biol Res; 1989; 306():51-67. PubMed ID: 2662213
[No Abstract] [Full Text] [Related]
6. Genetic counseling issues in the use of DNA analysis for Duchenne/Becker muscular dystrophy.
Cortada JM; Milsark I; Richards CS
Birth Defects Orig Artic Ser; 1990; 26(3):231-7. PubMed ID: 2092850
[No Abstract] [Full Text] [Related]
7. Carrier detection by DNA analysis in Duchenne muscular dystrophy families.
Battaloğlu E; Telatar M; Deymeer F; Serdaroğlu P; Ozdemir C; Kuseyri F; Apak MY; Tolun A
Turk J Pediatr; 1992; 34(2):79-92. PubMed ID: 1440954
[TBL] [Abstract][Full Text] [Related]
8. Germline mosaicism and Duchenne muscular dystrophy mutations.
Bakker E; Van Broeckhoven C; Bonten EJ; van de Vooren MJ; Veenema H; Van Hul W; Van Ommen GJ; Vandenberghe A; Pearson PL
Nature; 1987 Oct 8-14; 329(6139):554-6. PubMed ID: 2889144
[TBL] [Abstract][Full Text] [Related]
9. Genetic analysis of the Duchenne muscular dystrophy gene.
Prior TW
Arch Pathol Lab Med; 1991 Oct; 115(10):984-90. PubMed ID: 1898245
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. DNA analysis and genetic counselling in Duchenne muscular dystrophy.
Gardner RJ; Wilson SJ; Wilkins RJ
N Z Med J; 1988 Jul; 101(849):455-7. PubMed ID: 3399183
[TBL] [Abstract][Full Text] [Related]
13. DNA diagnostic tests in Xp21 dystrophy families for prenatal diagnosis.
Dinçer P; Topaloğlu H; Ayter S
Turk J Pediatr; 1998; 40(3):347-55. PubMed ID: 9763898
[TBL] [Abstract][Full Text] [Related]
14. Somatic mosaicism at the Duchenne locus.
Lebo RV; Olney RK; Golbus MS
Am J Med Genet; 1990 Oct; 37(2):187-90. PubMed ID: 1978985
[TBL] [Abstract][Full Text] [Related]
15. Carrier detection in Duchenne and Becker muscular dystrophy using dinucleotide repeat polymorphisms. A study in Mexican families.
Arenas D; Coral R; Cisneros B; Peñaloza L; Salamanca F; Kofman S; Mercado R; Méndez J; Martínez C; Montañez C
Arch Med Res; 1996; 27(2):151-6. PubMed ID: 8696057
[TBL] [Abstract][Full Text] [Related]
16. A molecular approach to genetic counseling in the X-linked muscular dystrophies.
Harper PS; Thomas NS
Am J Med Genet; 1986 Dec; 25(4):687-702. PubMed ID: 2878617
[TBL] [Abstract][Full Text] [Related]
17. Use of dystrophin genomic and cDNA probes for solving difficulties in carrier detection and prenatal diagnosis of Duchenne muscular dystrophy.
Shomrat R; Driks N; Legum C; Shiloh Y
Am J Med Genet; 1992 Feb; 42(3):281-7. PubMed ID: 1536162
[TBL] [Abstract][Full Text] [Related]
18. [Importance of germ cell mosaic for genetic counseling of families with Duchenne and Becker muscular dystrophy].
Janka M; Grimm T
Klin Padiatr; 1991; 203(5):354-8. PubMed ID: 1942941
[TBL] [Abstract][Full Text] [Related]
19. [Genetic counseling in Duchenne muscular dystrophy].
Martínez Matos JA
Neurologia; 1989 Oct; 4(8):265-7. PubMed ID: 2637768
[No Abstract] [Full Text] [Related]
20. Prenatal diagnosis and detection of carriers with DNA probes in Duchenne's muscular dystrophy.
Darras BT; Harper JF; Francke U
N Engl J Med; 1987 Apr; 316(16):985-92. PubMed ID: 3561454
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
