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 *

119 related articles for article (PubMed ID: 3355038)

  • 1. [Detection of carriers and diagnosis of Duchenne's muscular dystrophy by DNA analysis].
    Nunes Martínez V; Gallano Petit P; del Río Conde E; Casals Senent T; Baiget Bastus M
    An Esp Pediatr; 1988 Feb; 28(2):93-9. PubMed ID: 3355038
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. [Carrier detection and prenatal diagnosis of Duchenne's muscular dystrophy based on DNA analysis].
    Evgrafov OV; Badalian LO; Poliakov AV; Zaĭtseva SP; Malygina NA; Vinogradov SV; Bakharev VA; Mil'man FA; Lisova LP; Zaretskaia NV
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1990; 90(8):29-33. PubMed ID: 2175114
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [Carrier diagnosis and prenatal prognosis using DNA analysis in X-chromosome-linked Duchenne and Becker muscular dystrophy].
    Moser H; Liechti-Gallati S; Braga S; Hirsiger H
    Schweiz Med Wochenschr; 1987 Dec; 117(51):2061-73. PubMed ID: 3433090
    [TBL] [Abstract][Full Text] [Related]  

  • 7. DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.
    Bakker E; Bonten EJ; De Lange LF; Veenema H; Majoor-Krakauer D; Hofker MH; Van Ommen GJ; Pearson PL
    J Med Genet; 1986 Dec; 23(6):573-80. PubMed ID: 2879929
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Molecular biology in diagnosis and detection of deletion in Duchenne muscular dystrophy].
    Graninger W; Wintersberger W; Meron G; Smolen J; Toifl K; Vormittag W
    Wien Klin Wochenschr; 1991; 103(7):207-9. PubMed ID: 2063586
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Restriction polymorphism of 3 human genomic probes on the short arm of the X chromosome in a reference population, and applications in prenatal and carrier female diagnosis of Duchenne's muscular dystrophy].
    Dandieu S; Guérin P; Lucotte G
    C R Acad Sci III; 1985; 301(6):271-6. PubMed ID: 3928103
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Use of dystrophin c-DNA for the direct diagnosis of Duchenne muscular dystrophy in female carriers].
    Baiget M; del Río E; Gallano P
    Neurologia; 1989 Oct; 4(8):268-76. PubMed ID: 2576910
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Molecular diagnosis of Duchenne and Becker muscular dystrophies. Current data].
    Junien C; Boué J; Duros C; Coulon M; Cohen P; Dehaupas I; Gallano P; Léotard B; Nicolas H; Boué A
    Ann Genet; 1987; 30(1):5-16. PubMed ID: 3498430
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs.
    Bakker E; Hofker MH; Goor N; Mandel JL; Wrogemann K; Davies KE; Kunkel LM; Willard HF; Fenton WA; Sandkuyl L
    Lancet; 1985 Mar; 1(8430):655-8. PubMed ID: 2858615
    [TBL] [Abstract][Full Text] [Related]  

  • 13. DNA analysis of Duchenne and Becker muscular dystrophy using pERT87 genomic probes and dystrophin cDNA probes--establishing the optimum strategy for carrier diagnosis in the Japanese population.
    Ubagai T; Katayama S
    Jinrui Idengaku Zasshi; 1991 Sep; 36(3):211-27. PubMed ID: 1684391
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markers.
    Wilichowski E; Krawczak M; Seemanova E; Hanefeld F; Schmidtke J
    Hum Genet; 1987 Jan; 75(1):32-40. PubMed ID: 3026946
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Experience with DNA analysis in Duchenne and Becker muscular dystrophy families in NSW.
    Morgan G; Donald JA; Chen J; Serravalle S; Colley P; Denton MJ
    Aust Paediatr J; 1988; 24 Suppl 1():98-9. PubMed ID: 3202741
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Importance of germ cell mosaic for genetic counseling of families with Duchenne and Becker muscular dystrophy].
    Janka M; Grimm T
    Klin Padiatr; 1991; 203(5):354-8. PubMed ID: 1942941
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Service experience using DNA analysis for genetic prediction in Duchenne muscular dystrophy.
    Goodship J; Malcolm S; Robertson ME; Pembrey ME
    J Med Genet; 1988 Jan; 25(1):14-9. PubMed ID: 2895187
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Leber's congenital amaurosis with Duchenne's muscular dystrophy.
    Hazariwala K; Brownstein S; Polomeno R; Little JM; Labuda D
    Can J Ophthalmol; 1990 Jun; 25(4):202-7. PubMed ID: 1972344
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Application of DNA probes to carrier detection and prenatal diagnosis of Duchenne (and Becker) muscular dystrophy.
    Mulley JC; Gedeon AK; Haan EA; Sheffield LJ; White SJ; Bates LJ; Robertson EF; Sutherland GR
    Aust Paediatr J; 1988; 24 Suppl 1():92-7. PubMed ID: 3202740
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.