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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 26889671)

  • 21. [Clinical value of MLPA in the prenatal gene diagnosis of Duchenne muscular dystrophy].
    Li Q; Li SY; Zhang HM; He WZ; Ma XY; Wang XM; Xian JJ; Sun XF; Chen DJ; Yu YH
    Zhonghua Fu Chan Ke Za Zhi; 2013 Mar; 48(3):161-4. PubMed ID: 23849935
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Molecular prenatal diagnosis: the impact of modern technologies.
    Raymond FL; Whittaker J; Jenkins L; Lench N; Chitty LS
    Prenat Diagn; 2010 Jul; 30(7):674-81. PubMed ID: 20572117
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Rapid method for targeted prenatal diagnosis of Duchenne muscular dystrophy in Vietnam.
    Ta MH; Tran TH; Do NH; Pham le AT; Bui TH; Ta VT; Tran VK
    Taiwan J Obstet Gynecol; 2013 Dec; 52(4):534-9. PubMed ID: 24411039
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Best practice guidelines on molecular diagnostics in Duchenne/Becker muscular dystrophies.
    Abbs S; Tuffery-Giraud S; Bakker E; Ferlini A; Sejersen T; Mueller CR
    Neuromuscul Disord; 2010 Jun; 20(6):422-7. PubMed ID: 20466545
    [No Abstract]   [Full Text] [Related]  

  • 25. 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; 9(2):67-80. PubMed ID: 16137182
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [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]  

  • 27. [Mutation analysis and prenatal diagnosis for 50 pedigrees affected with Duchenne/Becker muscular dystrophy].
    Li H; Xu C; Mao Y; Lu J; Xiang Y; Xu X; Tang S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr; 35(2):169-174. PubMed ID: 29652985
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Maternal Plasma DNA and RNA Sequencing for Prenatal Testing.
    Tamminga S; van Maarle M; Henneman L; Oudejans CB; Cornel MC; Sistermans EA
    Adv Clin Chem; 2016; 74():63-102. PubMed ID: 27117661
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal diagnosis of Duchenne muscular dystrophy in 131 Chinese families with dystrophinopathy.
    Wang H; Xu Y; Liu X; Wang L; Jiang W; Xiao B; Wei W; Chen Y; Ye W; Ji X
    Prenat Diagn; 2017 Apr; 37(4):356-364. PubMed ID: 28181689
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination.
    Percesepe A; Ferrari M; Coviello D; Zanussi M; Castagni M; Neri I; Travi M; Forabosco A; Tedeschi S
    Prenat Diagn; 2005 Nov; 25(11):1011-4. PubMed ID: 16231306
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mosaicism in carrier of Duchenne muscular dystrophy mutation - Implication for prenatal diagnosis.
    Dinh LT; Nguyen DH; Luong LH; Le PT; Le-Anh TP; Tran DQ; Tran TH; Bui TH; Van Ta T; Tran VK
    Taiwan J Obstet Gynecol; 2018 Dec; 57(6):878-880. PubMed ID: 30545545
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prenatal diagnosis of Duchenne muscular dystrophy by comparative genomic hybridization.
    Bovolenta M; Rimessi P; Dolcini B; Ravani A; Ferlini A; Gualandi F
    Clin Genet; 2010 May; 77(5):503-6. PubMed ID: 20002456
    [No Abstract]   [Full Text] [Related]  

  • 33. Clinical application of fetal sex determination using cell-free fetal DNA in pregnant carriers of X-linked genetic disorders.
    Miura K; Higashijima A; Shimada T; Miura S; Yamasaki K; Abe S; Jo O; Kinoshita A; Yoshida A; Yoshimura S; Niikawa N; Yoshiura K; Masuzaki H
    J Hum Genet; 2011 Apr; 56(4):296-9. PubMed ID: 21307866
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Duchenne and Becker muscular dystrophy.
    Kneppers AL; Ginjaar IB; Bakker E
    Methods Mol Med; 2004; 92():311-41. PubMed ID: 14733319
    [No Abstract]   [Full Text] [Related]  

  • 35. [Prenatal diagnosis of Duchenne and Becker muscular dystrophy by multiplex ligation-dependent probe amplification].
    Wang Q; Jin CL; Lin CK; Cui WT; Ma HW; Wu YY
    Yi Chuan; 2009 Jun; 31(6):600-4. PubMed ID: 19586859
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Next Generation Sequencing approach to molecular diagnosis of Duchenne muscular dystrophy; identification of a novel mutation.
    Ebrahimzadeh-Vesal R; Teymoori A; Azimi-Nezhad M; Hosseini FS
    Gene; 2018 Feb; 644():1-3. PubMed ID: 29246534
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A novel and rapid mutation screening approach facilitates prenatal diagnosis.
    Ashton E; Deans Z; Yau SC; Abbs S
    Prenat Diagn; 2005 May; 25(5):425-6. PubMed ID: 15906416
    [No Abstract]   [Full Text] [Related]  

  • 38. Bioinformatics Approaches for Fetal DNA Fraction Estimation in Noninvasive Prenatal Testing.
    Peng XL; Jiang P
    Int J Mol Sci; 2017 Feb; 18(2):. PubMed ID: 28230760
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Genetic testing and prenatal diagnosis for eight families affected with Duchenne muscular dystrophy].
    Li Y; Zhang J; Xu Y; Guo F; Xu H; Yan F; Ren J; Wang D; Chen B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):363-6. PubMed ID: 26037351
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prenatal molecular diagnosis of inherited neuromuscular diseases: Duchenne/Becker muscular dystrophy, myotonic dystrophy type 1 and spinal muscular atrophy.
    Esposito G; Ruggiero R; Savarese M; Savarese G; Tremolaterra MR; Salvatore F; Carsana A
    Clin Chem Lab Med; 2013 Dec; 51(12):2239-45. PubMed ID: 23729582
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.