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.
131 related articles for article (PubMed ID: 28972564)
21. A splicing mutation in the DMD gene detected by next-generation sequencing and confirmed by mRNA and protein analysis. Roucher Boulez F; Menassa R; Streichenberger N; Manel V; Mallet-Motak D; Morel Y; Michel-Calemard L Clin Chim Acta; 2015 Aug; 448():146-9. PubMed ID: 26148721 [TBL] [Abstract][Full Text] [Related]
22. Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families - detection of carrier status in symptomatic and asymptomatic female relatives. Pikó H; Vancsó V; Nagy B; Bán Z; Herczegfalvi A; Karcagi V Neuromuscul Disord; 2009 Feb; 19(2):108-12. PubMed ID: 19084397 [TBL] [Abstract][Full Text] [Related]
23. Combining Protein Expression and Molecular Data Improves Mutation Characterization of Dystrophinopathies. Gaina G; Vossen RHAM; Manole E; Plesca DA; Ionica E Front Neurol; 2021; 12():718396. PubMed ID: 34950096 [TBL] [Abstract][Full Text] [Related]
24. Improved detection of deletions and duplications in the DMD gene using the multiplex ligation-dependent probe amplification (MLPA) method. Sansović I; Barišić I; Dumić K Biochem Genet; 2013 Apr; 51(3-4):189-201. PubMed ID: 23224783 [TBL] [Abstract][Full Text] [Related]
25. Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization. del Gaudio D; Yang Y; Boggs BA; Schmitt ES; Lee JA; Sahoo T; Pham HT; Wiszniewska J; Chinault AC; Beaudet AL; Eng CM Hum Mutat; 2008 Sep; 29(9):1100-7. PubMed ID: 18752307 [TBL] [Abstract][Full Text] [Related]
26. [Correlation between genotypes and phenotypes in pseudohypertrophic muscular dystrophy]. Feng SW; Liang YY; Cao JQ; Song XM; Zhang C Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec; 29(6):653-7. PubMed ID: 23225043 [TBL] [Abstract][Full Text] [Related]
27. Comprehensive Molecular Analysis of De Palma FDE; Nunziato M; D'Argenio V; Savarese M; Esposito G; Salvatore F Diagnostics (Basel); 2021 Oct; 11(10):. PubMed ID: 34679607 [TBL] [Abstract][Full Text] [Related]
28. Identification of deletions and duplications in the Duchenne muscular dystrophy gene and female carrier status in western India using combined methods of multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification. Dastur RS; Kachwala MY; Khadilkar SV; Hegde MR; Gaitonde PS Neurol India; 2011; 59(6):803-9. PubMed ID: 22234189 [TBL] [Abstract][Full Text] [Related]
29. Strategy for comprehensive molecular testing for Duchenne and Becker muscular dystrophies. Stockley TL; Akber S; Bulgin N; Ray PN Genet Test; 2006; 10(4):229-43. PubMed ID: 17253928 [TBL] [Abstract][Full Text] [Related]
30. [Detection of rare mutations in the dystrophin gene]. Zimowski JG; Holding M; Fidziańska E; Fidziańska A; Ryniewicz B; Dobosz I; Hausmanowa-Petrusewicz I; Kostera-Pruszczyk A; Zdzienicka E; Kubalska J; Andrzejczyk A; Zaremba J Med Wieku Rozwoj; 2009; 13(2):140-5. PubMed ID: 19837995 [TBL] [Abstract][Full Text] [Related]
31. Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center. Takeshima Y; Yagi M; Okizuka Y; Awano H; Zhang Z; Yamauchi Y; Nishio H; Matsuo M J Hum Genet; 2010 Jun; 55(6):379-88. PubMed ID: 20485447 [TBL] [Abstract][Full Text] [Related]
32. Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA). Gatta V; Scarciolla O; Gaspari AR; Palka C; De Angelis MV; Di Muzio A; Guanciali-Franchi P; Calabrese G; Uncini A; Stuppia L Hum Genet; 2005 Jun; 117(1):92-8. PubMed ID: 15841391 [TBL] [Abstract][Full Text] [Related]
33. Genetic Profile of the Dystrophin Gene Reveals New Mutations in Colombian Patients Affected with Muscular Dystrophinopathy. Triana-Fonseca P; Parada-Márquez JF; Silva-Aldana CT; Zambrano-Arenas D; Arias-Gomez LL; Morales-Fonseca N; Medina-Méndez E; Restrepo CM; Silgado-Guzmán DF; Fonseca-Mendoza DJ Appl Clin Genet; 2021; 14():399-408. PubMed ID: 34629887 [TBL] [Abstract][Full Text] [Related]
34. Molecular Genetics Analysis of 70 Chinese Families With Muscular Dystrophy Using Multiplex Ligation-Dependent Probe Amplification and Next-Generation Sequencing. Wang D; Gao M; Zhang K; Jin R; Lv Y; Liu Y; Ma J; Wan Y; Gai Z; Liu Y Front Pharmacol; 2019; 10():814. PubMed ID: 31404137 [No Abstract] [Full Text] [Related]
35. [Genetic diagnosis of Duchenne/Becker muscular dystrophy by MLPA]. Zhang Y; Liu X; He R; Ma H; Zhao Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun; 31(3):338-43. PubMed ID: 24928015 [TBL] [Abstract][Full Text] [Related]
36. [Clinical application of multiplex ligation-dependent probe amplification for the detection exonic copy number alterations in the Dystrophin gene]. Long F; Sun W; Ji X; Li XH; Liu XQ; Jiang WT; Tao J Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):699-704. PubMed ID: 22161109 [TBL] [Abstract][Full Text] [Related]
37. Use of in silico tools for classification of novel missense mutations identified in dystrophin gene in developing countries. Nouri N; Fazel-Najafabadi E; Behnam M; Nouri N; Aryani O; Ghasemi M; Nasiri J; Sedghi M Gene; 2014 Feb; 535(2):250-4. PubMed ID: 24274981 [TBL] [Abstract][Full Text] [Related]
38. DMD Mutations in 576 Dystrophinopathy Families: A Step Forward in Genotype-Phenotype Correlations. Juan-Mateu J; Gonzalez-Quereda L; Rodriguez MJ; Baena M; Verdura E; Nascimento A; Ortez C; Baiget M; Gallano P PLoS One; 2015; 10(8):e0135189. PubMed ID: 26284620 [TBL] [Abstract][Full Text] [Related]
39. Novel Intronic Mutations Introduce Pseudoexons in DMD That Cause Muscular Dystrophy in Patients. Lu X; Han C; Mai J; Jiang X; Liao J; Hou Y; Cui D Front Genet; 2021; 12():657040. PubMed ID: 33936175 [No Abstract] [Full Text] [Related]
40. Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene. Deburgrave N; Daoud F; Llense S; Barbot JC; Récan D; Peccate C; Burghes AH; Béroud C; Garcia L; Kaplan JC; Chelly J; Leturcq F Hum Mutat; 2007 Feb; 28(2):183-95. PubMed ID: 17041906 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]