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 *

134 related articles for article (PubMed ID: 2092848)

  • 21. Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels.
    den Dunnen JT; Bakker E; Breteler EG; Pearson PL; van Ommen GJ
    Nature; 1987 Oct 15-21; 329(6140):640-2. PubMed ID: 2889148
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. [Clinical molecular-genetics for endocrine and metabolic diseases].
    Niikawa N
    Rinsho Byori; 1989 Aug; 37(8):847-54. PubMed ID: 2573745
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. [Molecular and diagnostic genetics].
    Cochaux P; Velu T; Abramowicz M; Vassart G
    Rev Med Brux; 1990 Jun; 11(6):188-94. PubMed ID: 2196651
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The emerging genetic theories of unstable DNA, uniparental disomy, and imprinting.
    Wilkins-Haug L
    Curr Opin Obstet Gynecol; 1993 Apr; 5(2):179-85. PubMed ID: 8490087
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Update on the molecular genetics of Duchenne muscular dystrophy.
    Siddique T; Bartlett R; Pericak-Vance M; Yamaoka L; Koh J; Chen J; Hung WY; Kandt R; Roses AD
    Aust Paediatr J; 1988; 24 Suppl 1():9-14. PubMed ID: 3060079
    [TBL] [Abstract][Full Text] [Related]  

  • 28. DNA diagnostic tests in Xp21 dystrophy families for prenatal diagnosis.
    Dinçer P; Topaloğlu H; Ayter S
    Turk J Pediatr; 1998; 40(3):347-55. PubMed ID: 9763898
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prepregnancy testing for single-gene disorders by polar body analysis.
    Verlinsky Y; Rechitsky S; Verlinsky O; Ivachnenko V; Lifchez A; Kaplan B; Moise J; Valle J; Borkowski A; Nefedova J; Goltsman E; Strom C; Kuliev A
    Genet Test; 1999; 3(2):185-90. PubMed ID: 10464666
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Detection of exonic copy-number changes using a highly efficient oligonucleotide-based comparative genomic hybridization-array method.
    Saillour Y; Cossée M; Leturcq F; Vasson A; Beugnet C; Poirier K; Commere V; Sublemontier S; Viel M; Letourneur F; Barbot JC; Deburgrave N; Chelly J; Bienvenu T
    Hum Mutat; 2008 Sep; 29(9):1083-90. PubMed ID: 18683213
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genetics, amniocentesis, and abortion.
    Hirschhorn K
    Mt Sinai J Med; 1984; 51(1):15-7. PubMed ID: 6608672
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Reliable co-segregation analysis for prenatal diagnosis and heterozygote detection in Gaucher disease.
    Cormand B; Montfort M; Chabás A; Grinberg D; Vilageliu LL
    Prenat Diagn; 1998 Mar; 18(3):207-12. PubMed ID: 9556036
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetic screening for the next decade: application of present and new technologies.
    McCabe ER
    Yale J Biol Med; 1991; 64(1):9-14. PubMed ID: 1680260
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The use of DNA markers for carrier detection and prenatal diagnosis of haemophilia A in Egyptian families.
    Hussein IR; El-Beshlawy A; Salem A; Mosaad R; Zaghloul N; Ragab L; Fayek H; Gaber K; El-Ekiabi M
    Haemophilia; 2008 Sep; 14(5):1082-7. PubMed ID: 18547262
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Two buffer PAGE system-based SSCP/HD analysis: a general protocol for rapid and sensitive mutation screening in cystic fibrosis and any other human genetic disease.
    Liechti-Gallati S; Schneider V; Neeser D; Kraemer R
    Eur J Hum Genet; 1999 Jul; 7(5):590-8. PubMed ID: 10439967
    [TBL] [Abstract][Full Text] [Related]  

  • 36. DNA techniques in prenatal diagnosis and in genetic pathology.
    Rehder H; Friedrich U
    Am J Med Genet Suppl; 1987; 3():1-14. PubMed ID: 2897201
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Prenatal diagnosis of beta-thalassemia in the West Bank and Gaza.
    Ayesh SK; Al-Sharef WA; Nassar SM; Thawabteh NA; Abu-Libdeh BY
    Saudi Med J; 2005 Nov; 26(11):1771-6. PubMed ID: 16311664
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Genotypic diagnosis of Duchenne and Becker muscular dystrophies].
    Tuffery-Giraud S; Chambert S; Demaille J; Claustres M
    Ann Biol Clin (Paris); 1999; 57(4):417-26. PubMed ID: 10432364
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genetic counseling issues in the use of DNA analysis for Duchenne/Becker muscular dystrophy.
    Cortada JM; Milsark I; Richards CS
    Birth Defects Orig Artic Ser; 1990; 26(3):231-7. PubMed ID: 2092850
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.