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Items: 1 to 20 of 123

1.

[Molecular-genetic characteristics of mutations in dystrophin gene and clinical symptoms in Duchenne muscular dystrophy].

Lisiecka D, Wigowska-Sowińska J, Kwiatkowska J, Galas-Zgorzalewicz B, Słomski R.

Neurol Neurochir Pol. 1998 Sep-Oct;32(5):1069-79. Review. Polish.

PMID:
10463222
2.

Point mutation and polymorphism in Duchenne/Becker muscular dystrophy (D/BMD) patients.

Chaturvedi LS, Mukherjee M, Srivastava S, Mittal RD, Mittal B.

Exp Mol Med. 2001 Dec 31;33(4):251-6.

3.
4.

Detection of Duchenne and Becker muscular dystrophy carriers by quantitative multiplex polymerase chain reaction analysis.

Ioannou P, Christopoulos G, Panayides K, Kleanthous M, Middleton L.

Neurology. 1992 Sep;42(9):1783-90.

PMID:
1513470
5.
6.

Molecular analysis of the Duchenne muscular dystrophy gene in Spanish individuals: deletion detection and familial diagnosis.

Patiño A, Narbona J, García-Delgado M.

Am J Med Genet. 1995 Nov 6;59(2):182-7.

PMID:
8588583
8.

[Carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy by PCR methods].

Tsukamoto H, Inui K, Okada S.

Nihon Rinsho. 1993 Sep;51(9):2428-34. Review. Japanese.

PMID:
8105117
10.

Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: from Southern blot to protein truncation test.

Tuffery S, Chambert S, Bareil C, Sarda P, Coubes C, Echenne B, Demaille J, Claustres M.

Hum Genet. 1998 Mar;102(3):334-42.

PMID:
9544849
11.

[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. doi: 10.3760/cma.j.issn.1003-9406.2009.03.018. Chinese.

PMID:
19504448
12.

[Genotypic diagnosis of Duchenne and Becker muscular dystrophies].

Tuffery-Giraud S, Chambert S, Demaille J, Claustres M.

Ann Biol Clin (Paris). 1999 Jul-Aug;57(4):417-26. Review. French.

13.

Carrier detection in Duchenne muscular dystrophy using molecular methods.

Sakthivel Murugan SM, Arthi C, Thilothammal N, Lakshmi BR.

Indian J Med Res. 2013 Jun;137(6):1102-10.

14.

Dystrophin gene analysis and prenatal diagnosis of Duchenne muscular dystrophy in Russia.

Baranov VS, Gorbunova VN, Malysheva OV, Artemyeva OV, Kascheeva TK, Evgrafov OV, Polyakov AV, Lebedev VM, Kuznetzova TV, Shlykova SN, et al.

Prenat Diagn. 1993 May;13(5):323-33.

PMID:
8101987
15.

Experience and strategy for the molecular testing of Duchenne muscular dystrophy.

Prior TW, Bridgeman SJ.

J Mol Diagn. 2005 Aug;7(3):317-26. Review.

16.

DNA polymorphisms and deletion analysis of the Duchenne-Becker muscular dystrophy gene in the Chinese.

Soong BW, Tsai TF, Su CH, Kao KP, Hsiao KJ, Su TS.

Am J Med Genet. 1991 Mar 15;38(4):593-600.

PMID:
1676564
17.

[Analysis of deletions in the dystrophin gene in patients with Duchenne muscular dystrophy in the Bashkir Republic].

Grinchuk OV, Khidiiatova IM, Kiselev AV, Magzhanov RV, Khusnutdinova EK.

Genetika. 1999 Apr;35(4):551-5. Russian.

PMID:
10420280
18.

Splicing mutations in DMD/BMD detected by RT-PCR/PTT: detection of a 19AA insertion in the cysteine rich domain of dystrophin compatible with BMD.

Roest PA, Bout M, van der Tuijn AC, Ginjaar IB, Bakker E, Hogervorst FB, van Ommen GJ, den Dunnen JT.

J Med Genet. 1996 Nov;33(11):935-9.

19.

[Analysis of deletion mutations of the dystrophin gene by the multiplex polymerase chain reaction method in the diagnosis of Duchenne muscular dystrophy].

Baranov Vs, Gorbunova VN, Malysheva OV, Krasil'nikov VV.

Mol Gen Mikrobiol Virusol. 1991 Sep;(9):13-5. Russian.

PMID:
1745268
20.

Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy.

Schwartz LS, Tarleton J, Popovich B, Seltzer WK, Hoffman EP.

Am J Hum Genet. 1992 Oct;51(4):721-9.

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