BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

154 related articles for article (PubMed ID: 2906525)

  • 1. Identification of carriers of Duchenne muscular dystrophy: value of molecular analysis.
    LeRoy BS; Uhrhammer NA; Steere KJ; Boehm CD; King RA; Rich SS; Williams PP; Smith SA; de Martinville B
    Am J Med Genet; 1988 Nov; 31(3):709-21. PubMed ID: 2906525
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA.
    Darras BT; Koenig M; Kunkel LM; Francke U
    Am J Med Genet; 1988 Mar; 29(3):713-26. PubMed ID: 2897793
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Case of the month: germline mosaicism in carriers of Duchenne muscular dystrophy.
    Prior TW; Papp AC; Snyder PJ; Mendell JR
    Muscle Nerve; 1992 Aug; 15(8):960-3. PubMed ID: 1353862
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boy.
    Tuffery S; Moine P; Sarda P; Lefort G; Boulot P; Demaille J; Claustres M
    Genet Couns; 1994; 5(2):183-5. PubMed ID: 7917130
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.
    Sugino S; Fujishita S; Kamimura N; Matsumoto T; Wapenaar MC; Deng HX; Shibuya N; Miike T; Niikawa N
    Am J Med Genet; 1989 Dec; 34(4):555-61. PubMed ID: 2576185
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Carrier detection by DNA analysis in Duchenne muscular dystrophy families.
    Battaloğlu E; Telatar M; Deymeer F; Serdaroğlu P; Ozdemir C; Kuseyri F; Apak MY; Tolun A
    Turk J Pediatr; 1992; 34(2):79-92. PubMed ID: 1440954
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Somatic mosaicism at the Duchenne locus.
    Lebo RV; Olney RK; Golbus MS
    Am J Med Genet; 1990 Oct; 37(2):187-90. PubMed ID: 1978985
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic counseling of isolated carriers of Duchenne muscular dystrophy.
    Hoffman EP; Pegoraro E; Scacheri P; Burns RG; Taber JW; Weiss L; Spiro A; Blattner P
    Am J Med Genet; 1996 Jun; 63(4):573-80. PubMed ID: 8826437
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Use of dystrophin genomic and cDNA probes for solving difficulties in carrier detection and prenatal diagnosis of Duchenne muscular dystrophy.
    Shomrat R; Driks N; Legum C; Shiloh Y
    Am J Med Genet; 1992 Feb; 42(3):281-7. PubMed ID: 1536162
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Possibilities and problems in genomic diagnosis of Duchenne muscular dystrophy with molecular probes.
    Speer A; Davies K; McGlade S; Hanke R; Spiegler AW; Szibor R; Sommer D; Herrmann F; Coutelle C
    Biomed Biochim Acta; 1986; 45(7):K19-27. PubMed ID: 2878658
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis and detection of carriers with DNA probes in Duchenne's muscular dystrophy.
    Darras BT; Harper JF; Francke U
    N Engl J Med; 1987 Apr; 316(16):985-92. PubMed ID: 3561454
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Diagnosis and carrier detection in a Duchenne muscular dystrophy family by multiplex polymerase chain reaction and microsatellite analysis.
    Jongpiputvanich S; Norapucsunton T; Mutirangura A
    J Med Assoc Thai; 1996 Dec; 79 Suppl 1():S15-21. PubMed ID: 9071063
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular analysis of the Duchenne muscular dystrophy gene in Spanish individuals: deletion detection and familial diagnosis.
    Patiño A; Narbona J; García-Delgado M
    Am J Med Genet; 1995 Nov; 59(2):182-7. PubMed ID: 8588583
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Carrier detection and gene analysis in a Duchenne muscular dystrophy family].
    Lu FM
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1990 Aug; 23(4):231-3, 255. PubMed ID: 1979269
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Molecular biology in genetic counseling of Duchenne and Becker myopathy].
    Philip N; Voelckel MA; Girardot L; Lambert JC; Moncla A; Mattei JF; Giraud F
    Pediatrie; 1992; 47(12):821-8. PubMed ID: 1338927
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Heteroduplex analysis of the dystrophin gene: application to point mutation and carrier detection.
    Prior TW; Papp AC; Snyder PJ; Sedra MS; Western LM; Bartolo C; Moxley RT; Mendell JR
    Am J Med Genet; 1994 Mar; 50(1):68-73. PubMed ID: 8160755
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome.
    Wood S; Shukin RJ; McGillivray BC; Ray PN; Worton RG
    Am J Med Genet; 1988 Feb; 29(2):419-23. PubMed ID: 2895584
    [TBL] [Abstract][Full Text] [Related]  

  • 19. DNA analysis and genetic counselling in Duchenne muscular dystrophy.
    Gardner RJ; Wilson SJ; Wilkins RJ
    N Z Med J; 1988 Jul; 101(849):455-7. PubMed ID: 3399183
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Bayesian and RFLP linkage analysis on a DMD family].
    Gao YZ; Li MF; Zhang ZP; Zhang Q; Zhang LS; Wang SJ
    Yi Chuan Xue Bao; 1991; 18(4):300-3. PubMed ID: 1684713
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.