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Journal Abstract Search

285 related items for PubMed ID: 22830166

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. [Carrier genetic diagnosis of intron and/or exon-deletion Duchenne muscular dystrophy by microsatellite analysis and quantitative polymerase chain reaction].
    Huang W, Zhang C, Xie YM, Chen SL, Zhang WX, Yao XL, Zeng Y, Lu XL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Feb; 24(1):72-5. PubMed ID: 17285549
    [Abstract] [Full Text] [Related]

  • 3. [Efficiency of multiplex ligation-dependent probe amplification combined with short tandem repeat linkage analysis for the prenatal diagnosis for Duchenne muscular dystrophy].
    Li T, Wu D, Hou QF, Wang L, Guo QN, Kang B, Liu HY, Yang K, Ding XB, Liao SX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):40-4. PubMed ID: 23450477
    [Abstract] [Full Text] [Related]

  • 4. [Carrier detection of Duchenne/Becker muscular dystrophy by analysis of STRs loci linked to the gene of dystrophin in Venezuelan families].
    Delgado-Luengo WN, Borjas-Fuentes L, Zabala-Fernández W, Fernández-Salgado E, Solís-Añez E, Chávez C, Martínez-Basalo C, González-Ferrer S, Rojas-Atencio A, Morales-Machin A, Peña J, Pineda-Bernal L, González R, Miranda LE, Delgado-Luengo J, Hernández ML, Chacín JA, Quintero M.
    Invest Clin; 2002 Dec; 43(4):239-54. PubMed ID: 12520997
    [Abstract] [Full Text] [Related]

  • 5. Detection of Duchenne/Becker muscular dystrophy carriers in a group of Iranian families by linkage analysis.
    Malayeri FA, Panjehpour M, Movahedian A, Ghaffarpour M, Zamani GR, Tabrizi MH, Zamani M.
    Acta Med Iran; 2011 Dec; 49(3):142-8. PubMed ID: 21681700
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Platelet m-calpain: a facile marker and STR polymorphism analysis for the identification of true carriers of Duchenne muscular dystrophy.
    Mohana Rao V, Sridevi K, Anandraj MP.
    Integr Biol (Camb); 2012 Feb; 4(2):202-8. PubMed ID: 22166894
    [Abstract] [Full Text] [Related]

  • 8. Duchenne muscular dystrophy: a clinical, histopathological and genetic study at a neurology tertiary care center in Southern India.
    Swaminathan B, Shubha GN, Shubha D, Murthy AR, Kiran Kumar HB, Shylashree S, Gayathri N, Jamuna R, Jain S, Purushottam M, Nalini A.
    Neurol India; 2009 Feb; 57(6):734-8. PubMed ID: 20139501
    [Abstract] [Full Text] [Related]

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

  • 10. Serum Levels of MicroRNA-206 and Novel Mini-STR Assays for Carrier Detection in Duchenne Muscular Dystrophy.
    Anaya-Segura MA, Rangel-Villalobos H, Martínez-Cortés G, Gómez-Díaz B, Coral-Vázquez RM, Zamora-González EO, García S, López-Hernández LB.
    Int J Mol Sci; 2016 Aug 13; 17(8):. PubMed ID: 27529242
    [Abstract] [Full Text] [Related]

  • 11. 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 13; 52(4):534-9. PubMed ID: 24411039
    [Abstract] [Full Text] [Related]

  • 12. Carrier detection of Duchenne/Becker muscular dystrophy by using fluorescent linkage analysis in Taiwan.
    Lee CC, Wu MC, Wu JY, Li TC, Tsai FJ, Tsai CH.
    Acta Paediatr Taiwan; 2000 Dec 13; 41(2):69-74. PubMed ID: 10927942
    [Abstract] [Full Text] [Related]

  • 13. [Carrier detection of Duchenne/Becker muscular dystrophy in Chinese families by microsatellite analysis].
    Huang W, Zhang C, Xie YM, Chen SL, Zhang WX, Lu XL, Yao XL, Zeng Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Jun 13; 21(3):224-8. PubMed ID: 15192822
    [Abstract] [Full Text] [Related]

  • 14. [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 13; 77(2):103-9. PubMed ID: 19365952
    [Abstract] [Full Text] [Related]

  • 15. [Estimation of the probability of heterozygosity in Duchenne-type progressive muscular dystrophy].
    Guízar Vázquez J, Navarrete Cadena C, Rico R, Mora G, Zavala C.
    Bol Med Hosp Infant Mex; 1981 Feb 13; 38(1):23-33. PubMed ID: 7284070
    [Abstract] [Full Text] [Related]

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  • 17. Assessment of 6 STR loci for prenatal diagnosis of Duchenne Muscular Dystrophy.
    Dinh LT, Tran VK, Luong LH, Le PT, Nguyen AD, Thi Nguyen BS, Chi DV, Tran TH, Bui TH, Van Ta T, Nguyen DH.
    Taiwan J Obstet Gynecol; 2019 Sep 13; 58(5):645-649. PubMed ID: 31542086
    [Abstract] [Full Text] [Related]

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  • 19. 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 13; 25(13):1200-5. PubMed ID: 16353285
    [Abstract] [Full Text] [Related]

  • 20. [Analysis of short tandem repeat polymorphism in a female patient with Duchenne muscular dystrophy].
    Huang W, Zhang C, Chen SL, Feng HY, Zeng Y, Yao XL, Lu XL.
    Di Yi Jun Yi Da Xue Xue Bao; 2003 Oct 13; 23(10):1010-4. PubMed ID: 14559679
    [Abstract] [Full Text] [Related]

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