BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

346 related articles for article (PubMed ID: 19365952)

  • 1. [Prenatal molecular diagnosis of a DMD carrier female fetus by chorionic villus sampling and linkage analysis].
    Alcántara Ortigoza MA; Aguinaga Ríos M; González del Angel A; Zavaleta Abreu Mde J; Acevedo Gallegos S; Mayén Molina DG; del Castillo Ruíz V
    Ginecol Obstet Mex; 2009 Feb; 77(2):103-9. PubMed ID: 19365952
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis of DMD in a female foetus affected by Turner syndrome.
    Satre V; Monnier N; Devillard F; Amblard F; Lunardi J
    Prenat Diagn; 2004 Nov; 24(11):913-7. PubMed ID: 15565644
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. [Molecular genetic characteristics of Duchenne-Becker muscular dystrophy in the Republic of Moldova].
    Sacare VK
    Genetika; 2008 Oct; 44(10):1404-9. PubMed ID: 19062538
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Comparison of serum creatine kinase estimation with short tandem repeats based linkage analysis in carriers and affected children of Duchenne muscular dystrophy.
    Hashim R; Shaheen S; Ahmad S; Sattar A; Khan FA
    J Ayub Med Coll Abbottabad; 2011; 23(1):125-8. PubMed ID: 22830166
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Intragenic DNA polymorphism analysis of DMD/BMD dystrophy gene for carrier and prenatal diagnosis in 60 Iranian healthy individuals.
    Zamani M; Salahshour V; Kollaee A; Zamani GR; Sheidai M; Mohammadi M; Ghaffarpor M
    Int J Neurosci; 2011 Oct; 121(10):551-6. PubMed ID: 21774744
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chorionic villus sampling for early prenatal diagnosis at Bhumibol Adulyadej Hospital.
    Rueangchainikhom W; Sarapak S; Orungrote N
    J Med Assoc Thai; 2008 Jan; 91(1):1-6. PubMed ID: 18386536
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Prenatal diagnosis of Ullrich congenital muscular dystrophy using haplotype analysis and collagen VI immunocytochemistry.
    Brockington M; Brown SC; Lampe A; Yuva Y; Feng L; Jimenez-Mallebrera C; Sewry CA; Flanigan KM; Bushby K; Muntoni F
    Prenat Diagn; 2004 Jun; 24(6):440-4. PubMed ID: 15229843
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of Duchenne muscular dystrophy.
    Maheshwari M; Vijaya R; Kabra M; Arora S; Shastri SS; Deka D; Kriplani A; Menon PS
    Natl Med J India; 2000; 13(3):129-31. PubMed ID: 11558111
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 33(3):206-12. PubMed ID: 16553208
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Combining approach with multiplex PCR and MLPA to detect deletion and duplication in DMD patients, carriers, and prenatal diagnosis].
    Li H; Ding J; Wang W; Chen Y; Lu W; Shao H; Wu BL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):318-22. PubMed ID: 19504448
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical consequences of an increasing trend of preferential use of cultured villi for molecular diagnosis by CVS.
    Aina-Mumuney A; Wood ED; Corson VL; Stetten G; Jari S; Boehm CD; Blakemore KJ
    Prenat Diagn; 2008 Apr; 28(4):332-4. PubMed ID: 18330858
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Preimplantation genetic diagnosis (PGD) for Duchenne muscular dystrophy (DMD) by triplex-nested PCR.
    Malcov M; Ben-Yosef D; Schwartz T; Mey-Raz N; Azem F; Lessing JB; Amit A; Yaron Y
    Prenat Diagn; 2005 Dec; 25(13):1200-5. PubMed ID: 16353285
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of sickle cell anemia in twin pregnancies and identification by VNTRs.
    Attila G; Yalin S; Tuli A; Yalin E; Aksoy K
    Clin Chim Acta; 2004 Dec; 350(1-2):137-42. PubMed ID: 15530470
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis of muscle-eye-brain disease.
    Balci B; Morris-Rosendahl DJ; Celebi A; Talim B; Topaloglu H; Dinçer P
    Prenat Diagn; 2007 Jan; 27(1):51-4. PubMed ID: 17154333
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The association between chorionic villus sampling and preeclampsia.
    Grobman WA; Auger M; Shulman LP; Elias S
    Prenat Diagn; 2009 Aug; 29(8):800-3. PubMed ID: 19455602
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Non-invasive first trimester fetal gender assignment in pregnancies at risk for X-linked recessive diseases.
    Mazza V; Falcinelli C; Percesepe A; Paganelli S; Volpe A; Forabosco A
    Prenat Diagn; 2002 Oct; 22(10):919-24. PubMed ID: 12378578
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of alpha-thalassemia-1 (SEA type) by chorionic villus sampling.
    Chanprapaph P; Tongsong T; Wanapirak C; Sirichotiyakul S; Sanguansermsri T
    J Med Assoc Thai; 2002 Oct; 85(10):1049-53. PubMed ID: 12501894
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.