104 related articles for article (PubMed ID: 17251337)
1. A larger spectrum of intragenic short tandem repeats improves linkage analysis and localization of intragenic recombination detection in the dystrophin gene: an analysis of 93 families from southern Italy.
Carsana A; Frisso G; Tremolaterra MR; Ricci E; De Rasmo D; Salvatore F
J Mol Diagn; 2007 Feb; 9(1):64-9. PubMed ID: 17251337
[TBL] [Abstract][Full Text] [Related]
2. Carrier detection in non-deletional Duchenne/Becker muscular dystrophy families using polymorphic dinucleotide (CA) repeat loci of dystrophin gene.
Chaturvedi LS; Srivastava S; Mukherjee M; Mittal RD; Phadke SR; Pradhan S; Mittal B
Indian J Med Res; 2001 Jan; 113():19-25. PubMed ID: 11280167
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of Duchenne/Becker muscular dystrophy by short tandem repeat segregation analysis in Argentine families.
Giliberto F; Ferreiro V; Massot F; Ferrer M; Francipane L; Szijan I
Muscle Nerve; 2011 Apr; 43(4):510-7. PubMed ID: 21305566
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Detection of Duchenne/Becker muscular dystrophy carriers in a group of Iranian families by linkage analysis.
Malayeri FA; Panjehpour M; Movahedian A; Ghaffarpour M; Zamani GR; Tabrizi MH; Zamani M
Acta Med Iran; 2011; 49(3):142-8. PubMed ID: 21681700
[TBL] [Abstract][Full Text] [Related]
6. [Carrier detection of Duchenne/Becker muscular dystrophy by analysis of STRs loci linked to the gene of dystrophin in Venezuelan families].
Delgado-Luengo WN; Borjas-Fuentes L; Zabala-Fernández W; Fernández-Salgado E; Solís-Añez E; Chávez C; Martínez-Basalo C; González-Ferrer S; Rojas-Atencio A; Morales-Machin A; Peña J; Pineda-Bernal L; González R; Miranda LE; Delgado-Luengo J; Hernández ML; Chacín JA; Quintero M
Invest Clin; 2002 Dec; 43(4):239-54. PubMed ID: 12520997
[TBL] [Abstract][Full Text] [Related]
7. Intragenic DNA polymorphism analysis of DMD/BMD dystrophy gene for carrier and prenatal diagnosis in 60 Iranian healthy individuals.
Zamani M; Salahshour V; Kollaee A; Zamani GR; Sheidai M; Mohammadi M; Ghaffarpor M
Int J Neurosci; 2011 Oct; 121(10):551-6. PubMed ID: 21774744
[TBL] [Abstract][Full Text] [Related]
8. [Detecting carriers of a deletion in the dystrophin gene in families with a single case of Duchenne/Becker muscular dystrophy].
Bisko M; Zimowski JG; Hoffman-Zacharska D; Hausmanowa-Petrusewicz I; Fidziańska E; Zaremba J
Neurol Neurochir Pol; 1999; 33(6):1261-7. PubMed ID: 10791028
[TBL] [Abstract][Full Text] [Related]
9. Carrier detection of Duchenne/Becker muscular dystrophy by using fluorescent linkage analysis in Taiwan.
Lee CC; Wu MC; Wu JY; Li TC; Tsai FJ; Tsai CH
Acta Paediatr Taiwan; 2000; 41(2):69-74. PubMed ID: 10927942
[TBL] [Abstract][Full Text] [Related]
10. Molecular diagnosis of Duchenne/Becker muscular dystrophy by polymerase chain reaction and microsatellite analysis.
Kim UK; Chae JJ; Lee SH; Lee CC; Namkoong Y
Mol Cells; 2002 Jun; 13(3):385-8. PubMed ID: 12132577
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination.
Percesepe A; Ferrari M; Coviello D; Zanussi M; Castagni M; Neri I; Travi M; Forabosco A; Tedeschi S
Prenat Diagn; 2005 Nov; 25(11):1011-4. PubMed ID: 16231306
[TBL] [Abstract][Full Text] [Related]
14. Comparison of serum creatine kinase estimation with short tandem repeats based linkage analysis in carriers and affected children of Duchenne muscular dystrophy.
Hashim R; Shaheen S; Ahmad S; Sattar A; Khan FA
J Ayub Med Coll Abbottabad; 2011; 23(1):125-8. PubMed ID: 22830166
[TBL] [Abstract][Full Text] [Related]
15. Eight novel microsatellite markers in the 3' region of the dystrophin gene useful for diagnosis of Duchenne muscular dystrophy.
Matsumoto T; Niikawa N
Prenat Diagn; 2004 Dec; 24(12):1014-5. PubMed ID: 15612059
[No Abstract] [Full Text] [Related]
16. [A new approach to gene diagnosis of DMD/BMD--Amp-FLP linkage analysis].
Xu S
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1993 Dec; 15(6):405-10. PubMed ID: 7915972
[TBL] [Abstract][Full Text] [Related]
17. Molecular diagnosis of dystrophinopathies using a multi-technique analysis algorithm.
Luce LN; Ottaviani D; Ferrer M; Szijan I; Cotignola J; Giliberto F
Muscle Nerve; 2014 Feb; 49(2):249-56. PubMed ID: 23695957
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Identify female carriers and de novo mutations in deletional Duchenne/Becker muscular dystrophy families.
Zhu HY; Wu LQ; Liang DS; Pan Q; Xia JH
Yi Chuan Xue Bao; 2006 Mar; 33(3):206-12. PubMed ID: 16553208
[TBL] [Abstract][Full Text] [Related]
20. [Carrier's detection in families affected by Duchenne/Becker muscular dystrophy in which DNA from affected individuals is not available].
Bisko M; Zimowski JG; Fidziańska E; Zaremba J
Neurol Neurochir Pol; 1999; 33(6):1269-74. PubMed ID: 10791029
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
