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Journal Abstract Search
133 related items for PubMed ID: 1671720
1. Duchenne muscular dystrophy--a molecular service. Ballo R, Hitzeroth HW, Beighton PH. S Afr Med J; 1991 Feb 16; 79(4):209-12. PubMed ID: 1671720 [Abstract] [Full Text] [Related]
2. 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 07; 154(1):14-8. PubMed ID: 1670611 [Abstract] [Full Text] [Related]
3. Identification of Duchenne muscular dystrophy genomic probe P20 constant Taql fragment corresponding to the EcoRV and Mspl polymorphisms. Laing NG, Walker AP, Akkari PA, Chandler DC, Layton MG, Mears ME, Yamada T, Bartlett RJ, Pericak-Vance MA, Hung WY. Prenat Diagn; 1991 Jan 07; 11(1):63-7. PubMed ID: 1709287 [Abstract] [Full Text] [Related]
10. 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 07; 36(3):441-5. PubMed ID: 1968788 [Abstract] [Full Text] [Related]
11. DNA analysis of Duchenne and Becker muscular dystrophy using pERT87 genomic probes and dystrophin cDNA probes--establishing the optimum strategy for carrier diagnosis in the Japanese population. Ubagai T, Katayama S. Jinrui Idengaku Zasshi; 1991 Sep 07; 36(3):211-27. PubMed ID: 1684391 [Abstract] [Full Text] [Related]
13. 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 07; 37(6):456-62. PubMed ID: 2200624 [Abstract] [Full Text] [Related]
15. Prenatal diagnosis of Duchenne muscular dystrophy by DNA analysis. Old JM, Davies KE. J Med Genet; 1986 Dec 07; 23(6):556-9. PubMed ID: 2879927 [Abstract] [Full Text] [Related]
18. 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 07; 24(6):351-3. PubMed ID: 2907402 [Abstract] [Full Text] [Related]