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9. 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]
10. A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome. Wood S; Shukin RJ; McGillivray BC; Ray PN; Worton RG Am J Med Genet; 1988 Feb; 29(2):419-23. PubMed ID: 2895584 [TBL] [Abstract][Full Text] [Related]
11. Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boy. Tuffery S; Moine P; Sarda P; Lefort G; Boulot P; Demaille J; Claustres M Genet Couns; 1994; 5(2):183-5. PubMed ID: 7917130 [TBL] [Abstract][Full Text] [Related]
12. [Molecular biology in diagnosis and detection of deletion in Duchenne muscular dystrophy]. Graninger W; Wintersberger W; Meron G; Smolen J; Toifl K; Vormittag W Wien Klin Wochenschr; 1991; 103(7):207-9. PubMed ID: 2063586 [TBL] [Abstract][Full Text] [Related]
13. [Etiology of numerical and structural aberrations of the X chromosome. A study with highly polymorphic DNA markers]. Lorda-Sanchez I; Schinzel AA Ergeb Inn Med Kinderheilkd; 1993; 61():57-121. PubMed ID: 7900996 [No Abstract] [Full Text] [Related]
14. [New aspects of carrier diagnosis and human genetic counseling in Duchenne and Becker muscular dystrophy]. Spiegler AW; Huppert P; Werner W; Metzke H; Strobel U; Köhler K; Gerhardt R; Kaufmann J; Herrmann FH Z Arztl Fortbild (Jena); 1988; 82(22):1139-42. PubMed ID: 3247797 [No Abstract] [Full Text] [Related]
15. [Differential diagnosis of a benign course of muscular dystrophy using molecular genetic methods]. Wagner M; Diedrich U; Pozsàr C; Becker PE; Reiss J Nervenarzt; 1990 Apr; 61(4):244-7. PubMed ID: 2352571 [No Abstract] [Full Text] [Related]
16. [Presentation of a complex monitoring and therapy program in neuromuscular diseases, exemplified by X chromosomal muscular dystrophies. 1: Etiology, development, clinical and paraclinical findings]. Hoffmann W; Ullrich KP Padiatr Grenzgeb; 1987; 26(4):271-8. PubMed ID: 3658476 [No Abstract] [Full Text] [Related]
17. Linkage analyses in families with nephrogenic diabetes insipidus. Knoers NV; van der Heyden H; van Oost BA; Monnens L; Willems J; Ropers HH Prog Clin Biol Res; 1989; 305():149-55. PubMed ID: 2569742 [No Abstract] [Full Text] [Related]
18. [Principles of DNA diagnosis]. Moser H Klin Monbl Augenheilkd; 1990 May; 196(5):265-8. PubMed ID: 2366450 [TBL] [Abstract][Full Text] [Related]
19. [Use of DNA analysis in the prevention of progressive muscular dystrophies]. Kádasi L; Ferák V; Thurzová M; Kvasnicová M Bratisl Lek Listy; 1988 Nov; 89(11):828-34. PubMed ID: 2904832 [No Abstract] [Full Text] [Related]
20. [DNA markers, genetic counseling and prenatal diagnosis of hereditary disease. A study of 3 families with Duchenne's muscular dystrophy]. Schwartz M; Nørby S; Brandt NJ Ugeskr Laeger; 1985 Jun; 147(26):2071-5. PubMed ID: 3863357 [No Abstract] [Full Text] [Related] [Next] [New Search]