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.
49 related articles for article (PubMed ID: 2325103)
1. Novel mutation in spectrin-like repeat 1 of dystrophin central domain causes protein misfolding and mild Becker muscular dystrophy. Acsadi G; Moore SA; Chéron A; Delalande O; Bennett L; Kupsky W; El-Baba M; Le Rumeur E; Hubert JF J Biol Chem; 2012 May; 287(22):18153-62. PubMed ID: 22453924 [TBL] [Abstract][Full Text] [Related]
2. Two children with muscular dystrophies ascertained due to referral for diagnosis of autism. Zwaigenbaum L; Tarnopolsky M J Autism Dev Disord; 2003 Apr; 33(2):193-9. PubMed ID: 12757359 [TBL] [Abstract][Full Text] [Related]
5. The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II. Correlation of phenotype with genetic and protein abnormalities. Bushby KM; Gardner-Medwin D; Nicholson LV; Johnson MA; Haggerty ID; Cleghorn NJ; Harris JB; Bhattacharya SS J Neurol; 1993 Feb; 240(2):105-12. PubMed ID: 8437017 [TBL] [Abstract][Full Text] [Related]
6. Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 2. Correlations within individual patients. Nicholson LV; Johnson MA; Bushby KM; Gardner-Medwin D; Curtis A; Ginjaar IB; den Dunnen JT; Welch JL; Butler TJ; Bakker E J Med Genet; 1993 Sep; 30(9):737-44. PubMed ID: 8411068 [TBL] [Abstract][Full Text] [Related]
7. Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 1. Trends across the clinical groups. Nicholson LV; Johnson MA; Bushby KM; Gardner-Medwin D; Curtis A; Ginjaar IB; den Dunnen JT; Welch JL; Butler TJ; Bakker E J Med Genet; 1993 Sep; 30(9):728-36. PubMed ID: 8411067 [TBL] [Abstract][Full Text] [Related]
8. Direct detection of dystrophin gene rearrangements by analysis of dystrophin mRNA in peripheral blood lymphocytes. Roberts RG; Barby TF; Manners E; Bobrow M; Bentley DR Am J Hum Genet; 1991 Aug; 49(2):298-310. PubMed ID: 1867192 [TBL] [Abstract][Full Text] [Related]
9. Identification of a mutation in the promoter region of the dystrophin gene in a patient with atypical Becker muscular dystrophy. Bushby KM; Cleghorn NJ; Curtis A; Haggerty ID; Nicholson LV; Johnson MA; Harris JB; Bhattacharya SS Hum Genet; 1991 Dec; 88(2):195-9. PubMed ID: 1757094 [TBL] [Abstract][Full Text] [Related]
11. DNA analysis in Turkish Duchenne/Becker muscular dystrophy families. Battaloğlu E; Telatar M; Deymeer F; Serdaroğlu P; Kuseyri F; Ozdemir C; Apak M; Tolun A Hum Genet; 1992 Aug; 89(6):635-9. PubMed ID: 1355068 [TBL] [Abstract][Full Text] [Related]
12. 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; 37(6):456-62. PubMed ID: 2200624 [TBL] [Abstract][Full Text] [Related]
13. Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies. Claustres M; Tuffery S; Chevron MP; Jozelon MP; Martinez P; Echenne B; Demaille J Hum Genet; 1991 Dec; 88(2):179-84. PubMed ID: 1684565 [TBL] [Abstract][Full Text] [Related]
14. Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophies: deletion study and carrier detection. Asano J; Tomatsu S; Sukegawa K; Ikedo Y; Minami R; Iida M; Nishimura M; Nakagawa M; Ohshiro M; Orii T Clin Genet; 1991 Jun; 39(6):419-24. PubMed ID: 1863988 [TBL] [Abstract][Full Text] [Related]