399 related articles for article (PubMed ID: 11933457)
1. [Detection of carriers of Duchenne and Becker muscular dystrophy using the fluorescence in situ hybridization method].
Hermanová M; Lukás Z; Kroupová I; Lukásová E
Cesk Patol; 2002 Jan; 38(1):18-23. PubMed ID: 11933457
[TBL] [Abstract][Full Text] [Related]
2. Identification of female carriers for Duchenne and Becker muscular dystrophies using a FISH-based approach.
Ligon AH; Kashork CD; Richards CS; Shaffer LG
Eur J Hum Genet; 2000 Apr; 8(4):293-8. PubMed ID: 10854113
[TBL] [Abstract][Full Text] [Related]
3. Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization.
Rosenberg C; Navajas L; Vagenas DF; Bakker E; Vainzof M; Passos-Bueno MR; Takata RI; Van Ommen GJ; Zatz M; Den Dunnen JT
Neuromuscul Disord; 1998 Oct; 8(7):447-52. PubMed ID: 9829273
[TBL] [Abstract][Full Text] [Related]
4. Deletion analysis of the dystrophin gene in Duchenne and Becker muscular dystrophy patients: use in carrier diagnosis.
Kumari D; Mital A; Gupta M; Goyle S
Neurol India; 2003 Jun; 51(2):223-6. PubMed ID: 14571009
[TBL] [Abstract][Full Text] [Related]
5. [Detection of the gene-deleted female carriers of Duchenne/Becker muscular dystrophy using a fluorescent in situ hybridization based method].
Qi QW; Sun NH; Hao N
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):350-2. PubMed ID: 12903051
[TBL] [Abstract][Full Text] [Related]
6. 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; 12(5):353-6. PubMed ID: 16608904
[TBL] [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; 26(3):318-22. PubMed ID: 19504448
[TBL] [Abstract][Full Text] [Related]
8. Identification of duchenne muscular dystrophy female carriers by fluorescence in situ hybridization and RT-PCR.
Velázquez-Wong AC; Hernández-Huerta C; Márquez-Calixto A; Hernández-Aguilar FO; Rodríguez-Cruz M; Salamanca-Gómez F; Coral-Vázquez R
Genet Test; 2008 Jun; 12(2):221-3. PubMed ID: 18471087
[TBL] [Abstract][Full Text] [Related]
9. [Carrier detection in families affected by Duchenne/Becker muscular dystrophy].
Pikó H; Nagy B; Balog J; Bán Z; Herczegfalvi A; Karcagi V
Orv Hetil; 2007 Dec; 148(51):2403-9. PubMed ID: 18055393
[TBL] [Abstract][Full Text] [Related]
10. 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; 51(3-4):189-201. PubMed ID: 23224783
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA).
Gatta V; Scarciolla O; Gaspari AR; Palka C; De Angelis MV; Di Muzio A; Guanciali-Franchi P; Calabrese G; Uncini A; Stuppia L
Hum Genet; 2005 Jun; 117(1):92-8. PubMed ID: 15841391
[TBL] [Abstract][Full Text] [Related]
13. Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families - detection of carrier status in symptomatic and asymptomatic female relatives.
Pikó H; Vancsó V; Nagy B; Bán Z; Herczegfalvi A; Karcagi V
Neuromuscul Disord; 2009 Feb; 19(2):108-12. PubMed ID: 19084397
[TBL] [Abstract][Full Text] [Related]
14. 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; 23(12):1478-82. PubMed ID: 12518196
[TBL] [Abstract][Full Text] [Related]
15. Duchenne and Becker muscular dystrophy: a molecular and immunohistochemical approach.
Freund AA; Scola RH; Arndt RC; Lorenzoni PJ; Kay CK; Werneck LC
Arq Neuropsiquiatr; 2007 Mar; 65(1):73-6. PubMed ID: 17420831
[TBL] [Abstract][Full Text] [Related]
16. Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patients.
Lee T; Takeshima Y; Kusunoki N; Awano H; Yagi M; Matsuo M; Iijima K
J Hum Genet; 2014 Jan; 59(1):46-50. PubMed ID: 24225992
[TBL] [Abstract][Full Text] [Related]
17. Analysis of dystrophin gene in Iranian Duchenne and Becker muscular dystrophies patients and identification of a novel mutation.
Zamani GR; Karami F; Mehdizadeh M; Movafagh A; Nilipour Y; Zamani M
Neurol Sci; 2015 Nov; 36(11):2011-7. PubMed ID: 26081009
[TBL] [Abstract][Full Text] [Related]
18. 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; 33(4):251-6. PubMed ID: 11795488
[TBL] [Abstract][Full Text] [Related]
19. Genetic analysis of dystrophin gene for affected male and female carriers with Duchenne/Becker muscular dystrophy in Korea.
Lee BL; Nam SH; Lee JH; Ki CS; Lee M; Lee J
J Korean Med Sci; 2012 Mar; 27(3):274-80. PubMed ID: 22379338
[TBL] [Abstract][Full Text] [Related]
20. MLPA Analyses Reveal a Spectrum of Dystrophin Gene Deletions/Duplications in Pakistani Patients Suspected of Having Duchenne/Becker Muscular Dystrophy: A Retrospective Study.
Ansar Z; Nasir A; Moatter T; Khan S; Kirmani S; Ibrahim S; Imam K; Ather A; Samreen A; Hasan Z
Genet Test Mol Biomarkers; 2019 Jul; 23(7):468-472. PubMed ID: 31157985
[No Abstract] [Full Text] [Related]
[Next] [New Search]
