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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 9829273)

  • 1. 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]  

  • 2. [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]  

  • 3. 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]  

  • 4. 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]  

  • 5. DMD-specific FISH probes are diagnostically useful in the detection of female carriers of DMD gene deletions.
    Voskova-Goldman A; Peier A; Caskey CT; Richards CS; Shaffer LG
    Neurology; 1997 Jun; 48(6):1633-8. PubMed ID: 9191779
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Direct carrier detection by in situ suppression hybridization with cosmid clones of the Duchenne/Becker muscular dystrophy locus.
    Ried T; Mahler V; Vogt P; Blonden L; van Ommen GJ; Cremer T; Cremer M
    Hum Genet; 1990 Oct; 85(6):581-6. PubMed ID: 2227948
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Multicolor fluorescence in situ hybridization on metaphase chromosomes and interphase Halo-preparations using cosmid and YAC clones for the simultaneous high resolution mapping of deletions in the dystrophin gene.
    Tocharoentanaphol C; Cremer M; Schröck E; Blonden L; Kilian K; Cremer T; Ried T
    Hum Genet; 1994 Mar; 93(3):229-35. PubMed ID: 8125473
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients.
    Shomrat R; Gluck E; Legum C; Shiloh Y
    Am J Med Genet; 1994 Feb; 49(4):369-73. PubMed ID: 8160727
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Deletions within the gene of dystrophin in Duchenne and Becker muscular dystrophy].
    Zimowski JG; Bisko M; Fidziańska E; Hausmanowa-Petrusewicz I; Badurska B; Borkowska J; Lusakowska A; Fidziańska A; Jezuita J; Zaremba J
    Neurol Neurochir Pol; 1993; 27(4):469-78. PubMed ID: 8247234
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Detection of mutation in dystrophin gene in Duchenne muscular dystrophy--multiplex PCR and Southern blot analysis].
    Kawamura J
    Nihon Rinsho; 1997 Dec; 55(12):3126-30. PubMed ID: 9436422
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 19504448
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Detection of extensive deletions and duplications in the dystrophin gene].
    Fajkusová L; Kuhrová V; Hájek J; Fajkus J
    Cas Lek Cesk; 1997 Mar; 136(5):148-50. PubMed ID: 9221188
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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. PubMed ID: 1415217
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. [Molecular genetic analysis of deletions in the Duchenne and Becker types of progressive muscular dystrophy].
    Kádasi L; Gécz J; Saksová L; Thurzová M
    Bratisl Lek Listy; 1993 May; 94(5):249-53. PubMed ID: 8173987
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction.
    Beggs AH; Koenig M; Boyce FM; Kunkel LM
    Hum Genet; 1990 Nov; 86(1):45-8. PubMed ID: 2253937
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 10420280
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Somatic mosaicism for a deletion of the dystrophin gene in a carrier of Becker muscular dystrophy.
    Voit T; Neuen-Jacob E; Mahler V; Jauch A; Cremer M
    Eur J Pediatr; 1992 Feb; 151(2):112-6. PubMed ID: 1537352
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 48(6):416-22. PubMed ID: 25482253
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.