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4. 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]
5. Possibilities and problems in genomic diagnosis of Duchenne muscular dystrophy with molecular probes. Speer A; Davies K; McGlade S; Hanke R; Spiegler AW; Szibor R; Sommer D; Herrmann F; Coutelle C Biomed Biochim Acta; 1986; 45(7):K19-27. PubMed ID: 2878658 [TBL] [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. 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]
8. DUCHEN: an interactive computer program for calculating heterozygosity (carrier) risks in X-linked recessive lethal diseases, and its application in Duchenne muscular dystrophy. Andrews DF; Brasher PM; Manchester KE; Percy ME; Rusk AC; Soltan HC; Trueman DW Am J Med Genet; 1986 Oct; 25(2):211-8. PubMed ID: 3777018 [TBL] [Abstract][Full Text] [Related]
9. Molecular analysis of the Duchenne muscular dystrophy gene in Spanish individuals: deletion detection and familial diagnosis. Patiño A; Narbona J; García-Delgado M Am J Med Genet; 1995 Nov; 59(2):182-7. PubMed ID: 8588583 [TBL] [Abstract][Full Text] [Related]
10. Genetic counseling of isolated carriers of Duchenne muscular dystrophy. Hoffman EP; Pegoraro E; Scacheri P; Burns RG; Taber JW; Weiss L; Spiro A; Blattner P Am J Med Genet; 1996 Jun; 63(4):573-80. PubMed ID: 8826437 [TBL] [Abstract][Full Text] [Related]
11. Making the most of multiple measurements in estimating carrier probability in Duchenne muscular dystrophy: the Bayesian incorporation of repeated measurements using logistic discrimination. Percy ME; Andrews DF; Brasher PM; Rusk AC Am J Med Genet; 1987 Apr; 26(4):851-61. PubMed ID: 3591827 [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. Duchenne muscular dystrophy and idiopathic hyperCKemia in a family causing confusion in genetic counselling. Bushby K; Goodship J; Haggerty D; Heald A; Walls T Am J Med Genet; 1996 Dec; 66(2):237-8. PubMed ID: 8958338 [No Abstract] [Full Text] [Related]
14. Carrier detection by microsatellite analysis of Duchenne/Becker muscular dystrophy in Hungarian families. Bachrati CZ; Somodi Z; Endreffy E; Kalmár T; Raskó I Ann Hum Genet; 1998 Nov; 62(Pt 6):511-20. PubMed ID: 10363129 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Estimation of the probability of heterozygosity in Duchenne-type progressive muscular dystrophy]. Guízar Vázquez J; Navarrete Cadena C; Rico R; Mora G; Zavala C Bol Med Hosp Infant Mex; 1981; 38(1):23-33. PubMed ID: 7284070 [TBL] [Abstract][Full Text] [Related]
17. [Detection of carriers and diagnosis of Duchenne's muscular dystrophy by DNA analysis]. Nunes Martínez V; Gallano Petit P; del Río Conde E; Casals Senent T; Baiget Bastus M An Esp Pediatr; 1988 Feb; 28(2):93-9. PubMed ID: 3355038 [TBL] [Abstract][Full Text] [Related]
18. Deletion analysis of Duchenne muscular dystrophy. Erdem H; Ayter S; Ozgüç M; Topçu M; Topaloğlu H; Renda Y Turk J Pediatr; 1993; 35(1):15-21. PubMed ID: 8236513 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Rapid DNA haplotyping using a multiplex heteroduplex approach: application to Duchenne muscular dystrophy carrier testing. Prior TW; Wenger GD; Papp AC; Snyder PJ; Sedra MS; Bartolo C; Moore JW; Highsmith WE Hum Mutat; 1995; 5(3):263-8. PubMed ID: 7599638 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]