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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

302 related items for PubMed ID: 29652985

  • 41. Genetic profile of Brazilian patients with dystrophinopathies.
    de Almeida PAD, Machado-Costa MC, Manzoli GN, Ferreira LS, Rodrigues MCS, Bueno LSM, Saute JAM, Pinto Vairo F, Matte US, Siebert M, Cossio SL, Macedo GS, Winckler PB, Becker MM, Magalhães LVB, Gonçalves MVM, Marrone CD, Nucci A, França MC.
    Clin Genet; 2017 Aug; 92(2):199-203. PubMed ID: 28116794
    [Abstract] [Full Text] [Related]

  • 42. MLPA Application in Clinical Diagnosis of DMD/BMD in Shanghai.
    Ji X, Zhang J, Xu Y, Long F, Sun W, Liu X, Chen Y, Jiang W.
    J Clin Lab Anal; 2015 Sep; 29(5):405-11. PubMed ID: 25131993
    [Abstract] [Full Text] [Related]

  • 43. The role of polymorphic short tandem (CA)n repeat loci segregation analysis in the detection of Duchenne muscular dystrophy carriers and prenatal diagnosis.
    Ferreiro V, Giliberto F, Francipane L, Szijan I.
    Mol Diagn; 2005 Sep; 9(2):67-80. PubMed ID: 16137182
    [Abstract] [Full Text] [Related]

  • 44. 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
    [Abstract] [Full Text] [Related]

  • 45. Comprehensive genetic diagnosis of patients with Duchenne/Becker muscular dystrophy (DMD/BMD) and pathogenicity analysis of splice site variants in the DMD gene.
    Yang YM, Yan K, Liu B, Chen M, Wang LY, Huang YZ, Qian YQ, Sun YX, Li HG, Dong MY.
    J Zhejiang Univ Sci B; 2013 Apr; 20(9):753-765. PubMed ID: 31379145
    [Abstract] [Full Text] [Related]

  • 46. Mutation spectrum analysis of Duchenne/Becker muscular dystrophy in 68 families in Kuwait: The era of personalized medicine.
    Mohammed F, Elshafey A, Al-Balool H, Alaboud H, Al Ben Ali M, Baqer A, Bastaki L.
    PLoS One; 2018 Apr; 13(5):e0197205. PubMed ID: 29847600
    [Abstract] [Full Text] [Related]

  • 47. MLPA based detection of mutations in the dystrophin gene of 180 Polish families with Duchenne/Becker muscular dystrophy.
    Zimowski JG, Massalska D, Holding M, Jadczak S, Fidziańska E, Lusakowska A, Kostera-Pruszczyk A, Kamińska A, Zaremba J.
    Neurol Neurochir Pol; 2014 Apr; 48(6):416-22. PubMed ID: 25482253
    [Abstract] [Full Text] [Related]

  • 48. Mutation Spectrum of Dystrophinopathies in India: Implications for Therapy.
    Kohli S, Saxena R, Thomas E, Singh K, Bijarnia Mahay S, Puri RD, Verma IC.
    Indian J Pediatr; 2020 Jul; 87(7):495-504. PubMed ID: 32358784
    [Abstract] [Full Text] [Related]

  • 49. [Detection of mutations causing Duchenne and Becker muscular dystrophies: multiplex polymerase chain reaction vs. Multiplex ligation dependent probe amplification].
    Huamán-Dianderas FD, Guevara-Fujita ML, Málaga DR, Estrada-Cuzcano A, Fujita R.
    Rev Peru Med Exp Salud Publica; 2019 Jul; 36(3):475-480. PubMed ID: 31800942
    [Abstract] [Full Text] [Related]

  • 50.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 51. [A predictive analysis of the association between clinical phenotypes and genotypes in children with Becker muscular dystrophy/Duchenne muscular dystrophy].
    Niu HH, Tao DY, Cheng SQ.
    Zhongguo Dang Dai Er Ke Za Zhi; 2020 Jun; 22(6):602-607. PubMed ID: 32571459
    [Abstract] [Full Text] [Related]

  • 52. Genetic testing for Duchenne/Becker muscular dystrophy in Johannesburg, South Africa.
    Kerr R, Robinson C, Essop FB, Krause A.
    S Afr Med J; 2013 Oct 10; 103(12 Suppl 1):999-1004. PubMed ID: 24300647
    [Abstract] [Full Text] [Related]

  • 53. NGS-based targeted sequencing identified six novel variants in patients with Duchenne/Becker muscular dystrophy from southwestern China.
    Tang F, Xiao Y, Zhou C, Zhang H, Wang J, Zeng Y.
    BMC Med Genomics; 2023 May 30; 16(1):121. PubMed ID: 37254189
    [Abstract] [Full Text] [Related]

  • 54. Development of a comprehensive real-time PCR assay for dystrophin gene analysis and prenatal diagnosis of Chinese families.
    Zhang T, Liu S, Wei T, Yong J, Mao Y, Lu X, Xie J, Ke Q, Jin F, Qi M.
    Clin Chim Acta; 2013 Sep 23; 424():33-8. PubMed ID: 23680072
    [Abstract] [Full Text] [Related]

  • 55. Molecular analysis of the dystrophin gene in 407 Chinese patients with Duchenne/Becker muscular dystrophy by the combination of multiplex ligation-dependent probe amplification and Sanger sequencing.
    Chen WJ, Lin QF, Zhang QJ, He J, Liu XY, Lin MT, Murong SX, Liou CW, Wang N.
    Clin Chim Acta; 2013 Aug 23; 423():35-8. PubMed ID: 23588064
    [Abstract] [Full Text] [Related]

  • 56. Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patients.
    Dwianingsih EK, Iskandar K, Hapsara S, Ping Liu C, Malueka RG, Gunadi, Matsuo M, Lai PS.
    F1000Res; 2022 Aug 23; 11():148. PubMed ID: 38009102
    [Abstract] [Full Text] [Related]

  • 57. Characteristics of dystrophin gene mutations among Chinese patients as revealed by multiplex ligation-dependent probe amplification.
    Wang Q, Li-Ling J, Lin C, Wu Y, Sun K, Ma H, Jin C.
    Genet Test Mol Biomarkers; 2009 Feb 23; 13(1):23-30. PubMed ID: 19309270
    [Abstract] [Full Text] [Related]

  • 58. Rapid prenatal diagnosis of Duchenne muscular dystrophy with gene duplications by ion-pair reversed-phase high-performance liquid chromatography coupled with competitive multiplex polymerase chain reaction strategy.
    Huang WY, Hung CC, Lee CN, Su YN, Chen CP.
    Prenat Diagn; 2007 Jul 23; 27(7):653-6. PubMed ID: 17385798
    [Abstract] [Full Text] [Related]

  • 59. Investigation of genotype-phenotype and familial features of Turkish dystrophinopathy patients.
    Ozkalayci H, Bora E, Cankaya T, Kocabey M, Zubari NC, Yis U, Giray Bozkaya O, Turan S, Pekcanlar Akay A, Caglayan AO, Ulgenalp A.
    Neurogenetics; 2024 Jul 23; 25(3):201-213. PubMed ID: 38850354
    [Abstract] [Full Text] [Related]

  • 60. Identify female carriers and de novo mutations in deletional Duchenne/Becker muscular dystrophy families.
    Zhu HY, Wu LQ, Liang DS, Pan Q, Xia JH.
    Yi Chuan Xue Bao; 2006 Mar 23; 33(3):206-12. PubMed ID: 16553208
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 16.