304 related articles for article (PubMed ID: 29652985)
1. [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; 35(2):169-174. PubMed ID: 29652985
[TBL] [Abstract][Full Text] [Related]
2. [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
[TBL] [Abstract][Full Text] [Related]
3. [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
[TBL] [Abstract][Full Text] [Related]
4. [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
[TBL] [Abstract][Full Text] [Related]
5. [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; 54(4):226-231. PubMed ID: 31006187
[No 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
[TBL] [Abstract][Full Text] [Related]
7. 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; 20(1):139. PubMed ID: 31412794
[TBL] [Abstract][Full Text] [Related]
8. [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; 89(25):1753-6. PubMed ID: 19862979
[TBL] [Abstract][Full Text] [Related]
9. [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; 42(6):661-6. PubMed ID: 21170096
[TBL] [Abstract][Full Text] [Related]
10. [Mutation screening of 433 families with Duchenne/Becker muscular dystrophy].
Bai Y; Li S; Zong YN; Li XL; Zhao ZH; Kong XD
Zhonghua Yi Xue Za Zhi; 2016 Apr; 96(16):1261-9. PubMed ID: 27122458
[TBL] [Abstract][Full Text] [Related]
11. [Genetic testing and prenatal diagnosis of 671 Chinese pedigrees affected with Duchenne/Becker muscular dystrophy].
Luo S; He W; Zhao X; Yang X; Gao B; Li S; Du J; Zhang Q; Tan Y; Lu G; Lin G; Li W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Sep; 39(9):925-931. PubMed ID: 36082559
[TBL] [Abstract][Full Text] [Related]
12. Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center.
Zhang J; Ma D; Liu G; Wang Y; Liu A; Li L; Luo C; Hu P; Xu Z
BMC Med Genet; 2019 Nov; 20(1):180. PubMed ID: 31727011
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of 1408 foetuses at risk of DMD/BMD by MLPA and Sanger sequencing combined with STR linkage analysis.
Hua C; Liu L; Kong X
BMC Med Genomics; 2023 Dec; 16(1):310. PubMed ID: 38041114
[TBL] [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; 31(6):600-4. PubMed ID: 19586859
[TBL] [Abstract][Full Text] [Related]
15. 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
[TBL] [Abstract][Full Text] [Related]
16. 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; 38(1):53-6. PubMed ID: 16415967
[TBL] [Abstract][Full Text] [Related]
17. 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; 59(6):803-9. PubMed ID: 22234189
[TBL] [Abstract][Full Text] [Related]
18. Molecular Analysis-Based Genetic Characterization of a Cohort of Patients with Duchenne and Becker Muscular Dystrophy in Eastern China.
Zhao HH; Sun XP; Shi MC; Yi YX; Cheng H; Wang XX; Xu QC; Ma HM; Wu HQ; Jin QW; Niu Q
Chin Med J (Engl); 2018 Apr; 131(7):770-775. PubMed ID: 29578119
[TBL] [Abstract][Full Text] [Related]
19. 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
[TBL] [Abstract][Full Text] [Related]
20. Multiplex Ligation-Dependent Probe Amplification in X-linked Recessive Muscular Dystrophy in Korean Subjects.
Suh MR; Lee KA; Kim EY; Jung J; Choi WA; Kang SW
Yonsei Med J; 2017 May; 58(3):613-618. PubMed ID: 28332368
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]