PubMed

Similarity of DMD gene deletion and duplication in the Chinese patients compared to global populations.

Wang X, Wang Z, Yan M, Huang S, Chen TJ, Zhong N.

Behav Brain Funct. 2008 Apr 29;4:20.PMID: 18445268 [PubMed - in process]Related articlesFree article

[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. Chinese. PMID: 19504448 [PubMed - indexed for MEDLINE]Related articles

Detecting exon deletions and duplications of the DMD gene using Multiplex Ligation-dependent Probe Amplification (MLPA).

Lai KK, Lo IF, Tong TM, Cheng LY, Lam ST.

Clin Biochem. 2006 Apr;39(4):367-72. Epub 2006 Jan 17.PMID: 16413013 [PubMed - indexed for MEDLINE]Related articles

Small mutations detected by multiplex ligation-dependent probe amplification of the dystrophin gene.

Okizuka Y, Takeshima Y, Awano H, Zhang Z, Yagi M, Matsuo M.

Genet Test Mol Biomarkers. 2009 Jun;13(3):427-31.PMID: 19473085 [PubMed - indexed for MEDLINE]Related articles

Deletion and duplication screening in the DMD gene using MLPA.

Lalic T, Vossen RH, Coffa J, Schouten JP, Guc-Scekic M, Radivojevic D, Djurisic M, Breuning MH, White SJ, den Dunnen JT.

Eur J Hum Genet. 2005 Nov;13(11):1231-4.PMID: 16030524 [PubMed - indexed for MEDLINE]Related articlesFree article

Detection of deletions and duplications in the Duchenne muscular dystrophy gene by the molecular method MLPA in the first Argentine affected families.

Marzese DM, Mampel A, Gomez LC, Echeverria MI, Vargas AL, Ferreiro V, Giliberto F, Roqué M.

Genet Mol Res. 2008 Mar 11;7(1):223-33.PMID: 18393226 [PubMed - indexed for MEDLINE]Related articlesFree article

Gene diagnosis for nine Chinese patients with DMD/BMD by multiplex ligation-dependent probe amplification and prenatal diagnosis for one of them.

Wu Y, Yin G, Fu K, Wu D, Zhai Q, Du H, Huang Z, Niu Y.

J Clin Lab Anal. 2009;23(6):380-6.PMID: 19927354 [PubMed - in process]Related articles

Strategy for comprehensive molecular testing for Duchenne and Becker muscular dystrophies.

Stockley TL, Akber S, Bulgin N, Ray PN.

Genet Test. 2006 Winter;10(4):229-43.PMID: 17253928 [PubMed - indexed for MEDLINE]Related articles

Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients.

Dinçer P, Topaloğlu H, Ayter S, Ozgüç M, Taşdemir HA, Renda Y.

Brain Dev. 1996 Mar-Apr;18(2):91-4.PMID: 8733896 [PubMed - indexed for MEDLINE]Related articles

MLPA analysis for the detection of deletions, duplications and complex rearrangements in the dystrophin gene: potential and pitfalls.

Janssen B, Hartmann C, Scholz V, Jauch A, Zschocke J.

Neurogenetics. 2005 Feb;6(1):29-35. Epub 2005 Jan 18.PMID: 15655674 [PubMed - indexed for MEDLINE]Related articles

MLPA analysis/complete sequencing of the DMD gene in a group of Bulgarian Duchenne/Becker muscular dystrophy patients.

Todorova A, Todorov T, Georgieva B, Lukova M, Guergueltcheva V, Kremensky I, Mitev V.

Neuromuscul Disord. 2008 Aug;18(8):667-70. Epub 2008 Jul 23.PMID: 18653336 [PubMed - indexed for MEDLINE]Related articles

Sensitivity and frequencies of dystrophin gene mutations in Thai DMD/BMD patients as detected by multiplex PCR.

Sura T, Eu-ahsunthornwattana J, Pingsuthiwong S, Busabaratana M.

Dis Markers. 2008;25(2):115-21.PMID: 18957722 [PubMed - indexed for MEDLINE]Related articles

Integrated DNA, cDNA, and protein studies in Becker muscular dystrophy show high exception to the reading frame rule.

Kesari A, Pirra LN, Bremadesam L, McIntyre O, Gordon E, Dubrovsky AL, Viswanathan V, Hoffman EP.

Hum Mutat. 2008 May;29(5):728-37.PMID: 18348289 [PubMed - indexed for MEDLINE]Related articles

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;13(1):23-30.PMID: 19309270 [PubMed - indexed for MEDLINE]Related articles

A different spectrum of DMD gene mutations in local Chinese patients with Duchenne/Becker muscular dystrophy.

Lo IF, Lai KK, Tong TM, Lam ST.

Chin Med J (Engl). 2006 Jul 5;119(13):1079-87.PMID: 16834926 [PubMed - indexed for MEDLINE]Related articlesFree article

Deletion screening of the Duchenne/Becker muscular dystrophy gene in Croatian population.

Sertić J, Barisić N, Sostarko M, Brzović Z, Stavljenić-Rukavina A.

Coll Antropol. 1997 Jun;21(1):151-6.PMID: 9225508 [PubMed - indexed for MEDLINE]Related articles

[Evaluation of multiplex PCR assay using dual priming oligonucleotide system for detection mutation in the Duchenne muscular dystrophy gene]

Park Y, Kim J, Choi JR, Song J, Chung JS, Lee KA.

Korean J Lab Med. 2008 Oct;28(5):386-91. Korean. PMID: 18971620 [PubMed - indexed for MEDLINE]Related articlesFree article

[Detection of genomic duplications and deletions of the DMD gene in affected males and female carriers by using mutiplex ligation-dependent probe amplification]

Shen BC, Zhang C, Sun XF, Zhang HM, Li SY.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Aug;24(4):460-3. Chinese. PMID: 17680544 [PubMed - indexed for MEDLINE]Related articles

Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy.

Hodgson S, Hart K, Abbs S, Heckmatt J, Rodillo E, Bobrow M, Dubowitz V.

J Med Genet. 1989 Nov;26(11):682-93.PMID: 2585468 [PubMed - indexed for MEDLINE]Related articlesFree article

Analysis of dystrophin gene deletions by multiplex PCR in eastern India.

Basak J, Dasgupta UB, Banerjee TK, Senapati AK, Das SK, Mukherjee SC.

Neurol India. 2006 Sep;54(3):310-1.PMID: 16936400 [PubMed - indexed for MEDLINE]Related articlesFree article