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Journal Abstract Search

345 related items for PubMed ID: 16353285

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. [Preimplantation genetic diagnosis of Duchenne muscular dystrophy by single cell triplex PCR].
    Wu YL, Wu LQ, Li YP, Liu DE, Zeng Q, Zhu HY, Pan Q, Liang DS, Hu H, Long ZG, Li J, Dai HP, Xia K, Xia JH.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Apr; 32(2):246-51. PubMed ID: 17478931
    [Abstract] [Full Text] [Related]

  • 3. Multiplex nested PCR for preimplantation genetic diagnosis of spinal muscular atrophy.
    Malcov M, Schwartz T, Mei-Raz N, Yosef DB, Amit A, Lessing JB, Shomrat R, Orr-Urtreger A, Yaron Y.
    Fetal Diagn Ther; 2004 Apr; 19(2):199-206. PubMed ID: 14764971
    [Abstract] [Full Text] [Related]

  • 4. [Successful preimplantation genetic diagnosis for beta-thalassemia using multiplex nested polymerase chain reaction].
    Deng J, Zhuang GL, Peng WL, Zhou CQ, Li J, Liang XY, Deng MF, Zeng YH, Sun HY.
    Zhonghua Yi Xue Za Zhi; 2005 Mar 30; 85(12):811-5. PubMed ID: 15949396
    [Abstract] [Full Text] [Related]

  • 5. PGD for dystrophin gene deletions using fluorescence in situ hybridization.
    Malmgren H, White I, Johansson S, Levkov L, Iwarsson E, Fridström M, Blennow E.
    Mol Hum Reprod; 2006 May 30; 12(5):353-6. PubMed ID: 16608904
    [Abstract] [Full Text] [Related]

  • 6. Preimplantation genetic diagnosis for Duchenne muscular dystrophy by multiple displacement amplification.
    Ren Z, Zeng HT, Xu YW, Zhuang GL, Deng J, Zhang C, Zhou CQ.
    Fertil Steril; 2009 Feb 30; 91(2):359-64. PubMed ID: 18359022
    [Abstract] [Full Text] [Related]

  • 7. [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 30; 26(3):318-22. PubMed ID: 19504448
    [Abstract] [Full Text] [Related]

  • 8. [Single cell analysis of some deletion in dystrophin gene exons and gender determination by 3-plex nested PCR].
    Huang W, Zhang C, Xie YM, Chen SL, Jiao ZX, Zhou CQ, Zhang WX, Lu XL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Aug 30; 21(4):389-91. PubMed ID: 15300642
    [Abstract] [Full Text] [Related]

  • 9. Real-time reverse linkage using polar body analysis for preimplantation genetic diagnosis in female carriers of de novo mutations.
    Altarescu G, Eldar-Geva T, Varshower I, Brooks B, Haran EZ, Margalioth EJ, Levy-Lahad E, Renbaum P.
    Hum Reprod; 2009 Dec 30; 24(12):3225-9. PubMed ID: 19687056
    [Abstract] [Full Text] [Related]

  • 10. [Application of PCR technique in genetic diagnosis of Duchenne/Becker muscular dystrophy].
    Liu YM, Feng ZC, Fang ZW.
    Di Yi Jun Yi Da Xue Xue Bao; 2002 Aug 30; 22(8):731-3. PubMed ID: 12376264
    [Abstract] [Full Text] [Related]

  • 11. Mutation and haplotype analysis for Duchenne muscular dystrophy by single cell multiple displacement amplification.
    Ren Z, Zhou C, Xu Y, Deng J, Zeng H, Zeng Y.
    Mol Hum Reprod; 2007 Jun 30; 13(6):431-6. PubMed ID: 17439955
    [Abstract] [Full Text] [Related]

  • 12.
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    [No Abstract] [Full Text] [Related]

  • 13. Closely linked polymorphic marker: successful application in preimplantation genetic diagnosis for beta-thalassemia.
    Deng J, Zhuang GL, Peng WL, Zhou CQ, Li J, Fang C, Li SP, Chen Y, Tong DY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug 30; 22(4):391-5. PubMed ID: 16086275
    [Abstract] [Full Text] [Related]

  • 14. [Mutation analysis and prenatal diagnosis of sporadic DMD/BMD families].
    Zhu HY, Li J, Yang Y, Wu X, Zhu XY, Zhu RF, Zhang Y, Duan HL, Hu YL.
    Zhonghua Yi Xue Za Zhi; 2009 Jul 07; 89(25):1753-6. PubMed ID: 19862979
    [Abstract] [Full Text] [Related]

  • 15. Well-devised quantification analysis for duplication mutation of Duchenne muscular dystrophy aimed at preimplantation genetic diagnosis.
    Nakabayashi A, Sueoka K, Tajima H, Sato K, Sakamoto Y, Katou S, Yoshimura Y.
    J Assist Reprod Genet; 2007 Jun 07; 24(6):233-40. PubMed ID: 17340191
    [Abstract] [Full Text] [Related]

  • 16. [Results from 10 years of preimplantation-genetic diagnostics in The Netherlands].
    de Die-Smulders CE, Land JA, Dreesen JC, Coonen E, Evers JL, Geraedts JP.
    Ned Tijdschr Geneeskd; 2004 Dec 11; 148(50):2491-6. PubMed ID: 15638197
    [Abstract] [Full Text] [Related]

  • 17.
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  • 18. Duplex PCR for preimplantation genetic diagnosis (PGD) of spinal muscular atrophy.
    Moutou C, Gardes N, Viville S.
    Prenat Diagn; 2003 Aug 11; 23(8):685-9. PubMed ID: 12913876
    [Abstract] [Full Text] [Related]

  • 19. Deletion mutations in the dystrophin gene of Saudi patients with Duchenne and Becker muscular dystrophy.
    Al-Jumah M, Majumdar R, Al-Rajeh S, Chaves-Carballo E, Salih MM, Awada A, Al-Shahwan S, Al-Uthaim S.
    Saudi Med J; 2002 Dec 11; 23(12):1478-82. PubMed ID: 12518196
    [Abstract] [Full Text] [Related]

  • 20. Modification of the triplet repeat primed polymerase chain reaction method for detection of the CTG repeat expansion in myotonic dystrophy type 1: application in preimplantation genetic diagnosis.
    Kakourou G, Dhanjal S, Mamas T, Serhal P, Delhanty JD, SenGupta SB.
    Fertil Steril; 2010 Oct 11; 94(5):1674-9. PubMed ID: 20171614
    [Abstract] [Full Text] [Related]

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