These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
77 related articles for article (PubMed ID: 1461839)
1. [DMD gene--the largest human gene]. Kwiatkowska J; Słomski R Postepy Biochem; 1992; 38(2):49-55. PubMed ID: 1461839 [No Abstract] [Full Text] [Related]
2. [Clinical,manifestations of the myopathies due to deletions/mutations of the dystrophin gene]. Bonilla E; Minetti C; Chang HW; Medori R; Cordone G; Di Mauro S Minerva Pediatr; 1991 Mar; 43(3):67-70. PubMed ID: 1870528 [No Abstract] [Full Text] [Related]
3. Identification of a point mutation and germinal mosaicism in a Duchenne muscular dystrophy family. Wilton SD; Chandler DC; Kakulas BA; Laing NG Hum Mutat; 1994; 3(2):133-40. PubMed ID: 8199594 [TBL] [Abstract][Full Text] [Related]
4. Dystrophin deficiency in a case of congenital myopathy. Prelle A; Medori R; Moggio M; Chan HW; Gallanti A; Scarlato G; Bonilla E J Neurol; 1992 Feb; 239(2):76-8. PubMed ID: 1552307 [TBL] [Abstract][Full Text] [Related]
5. Molecular genetic and immunological analysis of dystrophin of a young patient with X-linked muscular dystrophy. Ikeya K; Saito K; Hayashi K; Tanaka H; Hagiwara Y; Yoshida M; Yamauchi A; Fukuyama Y; Ishiguro T; Eguchi C Am J Med Genet; 1992 Jun; 43(3):580-7. PubMed ID: 1605252 [TBL] [Abstract][Full Text] [Related]
6. Transcriptional profiles from patients with dystrophinopathies and limb girdle muscular dystrophies as determined by qRT-PCR. Arning L; Jagiello P; Schara U; Vorgerd M; Dahmen N; Gencikova A; Mortier W; Epplen JT; Gencik M J Neurol; 2004 Jan; 251(1):72-8. PubMed ID: 14999492 [TBL] [Abstract][Full Text] [Related]
7. Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studies. Vainzof M; Pavanello RC; Pavanello-Filho I; Rapaport D; Passos-Bueno MR; Zubrzycka-Gaarn EE; Bulman DE; Zatz M Am J Med Genet; 1991 Apr; 39(1):38-41. PubMed ID: 1867262 [TBL] [Abstract][Full Text] [Related]
8. Familial occurrence of Duchenne dystrophy through paternal lines in four families. Zatz M; Passos-Bueno MR; Rapaport D; Vainzof M Am J Med Genet; 1991 Jan; 38(1):80-4. PubMed ID: 1849353 [TBL] [Abstract][Full Text] [Related]
9. A model to estimate the expression of the dystrophin gene in muscle from female Becker muscular dystrophy carriers. Vainzof M; Passos-Bueno MR; Pavanello RC; Schreiber R; Zatz M J Med Genet; 1992 Jul; 29(7):476-9. PubMed ID: 1640426 [TBL] [Abstract][Full Text] [Related]
10. Detection of DMD gene deletions in Thai children patients. Kamolsilp M; Paditaporn R; Noonai A; Wasant P Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():172-4. PubMed ID: 8629100 [TBL] [Abstract][Full Text] [Related]
11. Interrelationship between gene, its product and phenotype in Duchenne and Becker muscular dystrophy. Hausmanowa-Petrusewicz I; Zaremba J; Fidziańska A; Zimowski J; Bisko M; Badurska B; Fidziańska E; Lusakowska A; Borkowska J Acta Neurobiol Exp (Wars); 1993; 53(1):297-303. PubMed ID: 8317263 [TBL] [Abstract][Full Text] [Related]
12. [DNA and dystrophin analysis in Duchenne's and Becker's disease; benefit to the patient]. Jennekens FG; Ippel PF Ned Tijdschr Geneeskd; 1993 Jan; 137(2):61-3. PubMed ID: 8421528 [No Abstract] [Full Text] [Related]
13. [Regulation of human DMD gene expression. An example of multiple utilization of genetic information]. Napierała D; Słomski R Postepy Biochem; 1998; 44(1):48-55. PubMed ID: 9738237 [No Abstract] [Full Text] [Related]
14. [Significance of dystrophin analysis in adult myopathies. Study methods, case reports and current pathogenetic considerations]. Gold R; Kress W; Meurers B; Müller CR; Reichmann H Nervenarzt; 1991 Jun; 62(6):360-8. PubMed ID: 1876220 [No Abstract] [Full Text] [Related]
16. In utero fetal muscle biopsy for the diagnosis of Duchenne muscular dystrophy in a female fetus "suddenly at risk". Evans MI; Farrell SA; Greb A; Ray P; Johnson MP; Hoffman EP Am J Med Genet; 1993 May; 46(3):309-12. PubMed ID: 8488877 [TBL] [Abstract][Full Text] [Related]
17. Somatic mosaicism for a DMD gene deletion. Saito K; Ikeya K; Kondo E; Komine S; Komine M; Osawa M; Aikawa E; Fukuyama Y Am J Med Genet; 1995 Mar; 56(1):80-6. PubMed ID: 7747792 [TBL] [Abstract][Full Text] [Related]