These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
490 related items for PubMed ID: 24928015
1. [Genetic diagnosis of Duchenne/Becker muscular dystrophy by MLPA]. Zhang Y, Liu X, He R, Ma H, Zhao Y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun; 31(3):338-43. PubMed ID: 24928015 [Abstract] [Full Text] [Related]
2. [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 [Abstract] [Full Text] [Related]
3. 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; 52(4):534-9. PubMed ID: 24411039 [Abstract] [Full Text] [Related]
4. [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 [Abstract] [Full Text] [Related]
5. Identification of deletions and duplications in the Duchenne muscular dystrophy gene and female carrier status in western India using combined methods of multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification. Dastur RS, Kachwala MY, Khadilkar SV, Hegde MR, Gaitonde PS. Neurol India; 2011 Mar; 59(6):803-9. PubMed ID: 22234189 [Abstract] [Full Text] [Related]
6. [Mutation analysis and prenatal diagnosis of families affected with Duchenne and Becker muscular dystrophy]. Wang WJ, Zhu HY, Zhu RF, Yang Y, Zhu XY, Duan HL, Zhang Y, Wu X. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):45-8. PubMed ID: 23450478 [Abstract] [Full Text] [Related]
7. Use of multiplex ligation-dependent probe amplification (MLPA) for Duchenne muscular dystrophy (DMD) gene mutation analysis. Murugan S, Chandramohan A, Lakshmi BR. Indian J Med Res; 2010 Sep; 132():303-11. PubMed ID: 20847377 [Abstract] [Full Text] [Related]
8. [Genetic analysis and prenatal diagnosis of Duchenne or Becker muscular dystrophy]. Zhao W, Jiang N, Li S, Li JS, Miao Y, Liang SY, Yu DY. Zhonghua Fu Chan Ke Za Zhi; 2019 Apr 25; 54(4):226-231. PubMed ID: 31006187 [Abstract] [Full Text] [Related]
9. Improved detection of deletions and duplications in the DMD gene using the multiplex ligation-dependent probe amplification (MLPA) method. Sansović I, Barišić I, Dumić K. Biochem Genet; 2013 Apr 25; 51(3-4):189-201. PubMed ID: 23224783 [Abstract] [Full Text] [Related]
10. Genetic diagnosis of Duchenne and Becker muscular dystrophy using multiplex ligation-dependent probe amplification in Rwandan patients. Uwineza A, Hitayezu J, Murorunkwere S, Ndinkabandi J, Kalala Malu CK, Caberg JH, Dideberg V, Bours V, Mutesa L. J Trop Pediatr; 2014 Apr 25; 60(2):112-7. PubMed ID: 24213305 [Abstract] [Full Text] [Related]
11. Genetic analysis of 1051 Chinese families with Duchenne/Becker Muscular Dystrophy. Kong X, Zhong X, Liu L, Cui S, Yang Y, Kong L. BMC Med Genet; 2019 Aug 14; 20(1):139. PubMed ID: 31412794 [Abstract] [Full Text] [Related]
12. A comparative study of mPCR, MLPA, and muscle biopsy results in a cohort of children with Duchenne muscular dystrophy: a first study. Manjunath M, Kiran P, Preethish-Kumar V, Nalini A, Singh RJ, Gayathri N. Neurol India; 2015 Aug 14; 63(1):58-62. PubMed ID: 25751470 [Abstract] [Full Text] [Related]
13. [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 14; 30(1):40-4. PubMed ID: 23450477 [Abstract] [Full Text] [Related]
14. [Prenatal diagnosis of Duchenne and Becker muscular dystrophy by multiplex ligation-dependent probe amplification]. Wang Q, Jin CL, Lin CK, Cui WT, Ma HW, Wu YY. Yi Chuan; 2009 Jun 14; 31(6):600-4. PubMed ID: 19586859 [Abstract] [Full Text] [Related]
15. [Mutation analysis and prenatal diagnosis for 50 pedigrees affected with Duchenne/Becker muscular dystrophy]. Li H, Xu C, Mao Y, Lu J, Xiang Y, Xu X, Tang S. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr 10; 35(2):169-174. PubMed ID: 29652985 [Abstract] [Full Text] [Related]
16. [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]
17. Prenatal molecular diagnosis of Duchenne and Becker muscular dystrophy. Li Q, Li SY, Hu DG, Sun XF, Chen DJ, Zhang C, Jiang WY. Beijing Da Xue Xue Bao Yi Xue Ban; 2006 Feb 18; 38(1):53-6. PubMed ID: 16415967 [Abstract] [Full Text] [Related]
18. [Genotype, phenotype analysis and follow-up study on patients with Duchenne/Becker muscular dystrophy]. Zhang YZ, Xiong H, Wang XZ, Wang S, Luo J, Wang JM, Jiang YW, Chang XZ, Pan H, Qi JG, Li WZ, Yuan Y, Wu XR. Beijing Da Xue Xue Bao Yi Xue Ban; 2010 Dec 18; 42(6):661-6. PubMed ID: 21170096 [Abstract] [Full Text] [Related]
19. MLPA based detection of mutations in the dystrophin gene of 180 Polish families with Duchenne/Becker muscular dystrophy. Zimowski JG, Massalska D, Holding M, Jadczak S, Fidziańska E, Lusakowska A, Kostera-Pruszczyk A, Kamińska A, Zaremba J. Neurol Neurochir Pol; 2014 Dec 18; 48(6):416-22. PubMed ID: 25482253 [Abstract] [Full Text] [Related]
20. 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 18; 13(11):1231-4. PubMed ID: 16030524 [Abstract] [Full Text] [Related] Page: [Next] [New Search]