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 *

161 related articles for article (PubMed ID: 8445619)

  • 21. Role of molecular biology in obstetrics--modern single gene disorders diagnosis techniques.
    Piyamongkol W
    J Med Assoc Thai; 2006 Oct; 89 Suppl 4():S186-91. PubMed ID: 17725155
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Danger of delay for genetic tests.
    Newmark P
    Nature; 1986 Jun 5-11; 321(6070):557. PubMed ID: 3520337
    [TBL] [Abstract][Full Text] [Related]  

  • 23. UK clinicians' knowledge of and attitudes to the prenatal diagnosis of single gene disorders.
    Firth HV; Lindenbaum RH
    J Med Genet; 1992 Jan; 29(1):20-3. PubMed ID: 1532425
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [New molecular technology in prenatal genetic diagnosis].
    Ben-Chetrit A; Yagel S; Friedman A
    Harefuah; 1991 Jul; 121(1-2):55-7. PubMed ID: 1748347
    [No Abstract]   [Full Text] [Related]  

  • 25. [The molecular diagnosis of hereditary diseases. In memoriam Dr. Eduardo Aguirre Pequeño].
    Barrera Saldaña HA; Rojas Martínez A; Rivera Pérez JA; Vázquez Alemán RM; González Garay ML
    Gac Med Mex; 1992; 128(6):613-20; discussion 620-1. PubMed ID: 1344797
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Carbon nanofiber-based multiplexed immunosensor for the detection of survival motor neuron 1, cystic fibrosis transmembrane conductance regulator and Duchenne Muscular Dystrophy proteins.
    Eissa S; Alshehri N; Abduljabbar M; Rahman AMA; Dasouki M; Nizami IY; Al-Muhaizea MA; Zourob M
    Biosens Bioelectron; 2018 Oct; 117():84-90. PubMed ID: 29890394
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [From people to molecules ... and back?].
    Galjaard H
    Ned Tijdschr Geneeskd; 1982 Dec; 126(51):2335-43. PubMed ID: 6218414
    [No Abstract]   [Full Text] [Related]  

  • 28. Molecular genetics in clinical practice: evolution of a DNA diagnostic service.
    Meredith AL; Upadhyaya M; Harper PS
    BMJ; 1988 Oct; 297(6652):843-6. PubMed ID: 2972330
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Molecular genetic studies in monogenic and polygenic human diseases.
    Endreffy E; László ; Szabó A; Román F; Kürti K; Kálmán M; Raskó I
    Acta Biol Hung; 1997; 48(1):121-8. PubMed ID: 9199707
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [The progress and strategy of molecular diagnosis for human genetic diseases].
    Nanba E
    No To Hattatsu; 1998 Mar; 30(2):123-7. PubMed ID: 9545776
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Recent advances in human molecular genetics].
    Abe T
    Rinsho Byori; 1990 Oct; 38(10):1093-100. PubMed ID: 1979824
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Prenatal diagnosis of genetic diseases in France].
    Mathieu M
    Ann Pharm Fr; 1999 Sep; 57(5):380-4. PubMed ID: 10520508
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [First attempts in preimplantation genetic diagnosis: genetic analysis].
    Bán Z; Fancsovits P; Nagy B; Kamaszné HM; Urbancsek J; Papp Z
    Orv Hetil; 2001 Nov; 142(45):2487-92. PubMed ID: 11778356
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Advances in molecular diagnosis.
    Korf BR
    Curr Opin Obstet Gynecol; 1996 Apr; 8(2):130-4. PubMed ID: 8734129
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Preimplantation genetic diagnosis of monogenic diseases].
    Moutou C; Viville S
    Ann Biol Clin (Paris); 2003; 61(5):521-32. PubMed ID: 14671749
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [New frontiers in noninvasive, prenatal screening and diagnosis: fetal DNA circulating in maternal blood].
    Montagnana M; Lippi G; Guidi GC
    Minerva Ginecol; 2007 Jun; 59(3):331-41. PubMed ID: 17576408
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Antenatal diagnosis of haemoglobinopathies, haemophilia, von Willebrand's disease, Duchenne's muscular dystrophy, and chronic granulomatous disease by fetal blood analysis.
    DeVore GR; Mahoney MJ; Hobbins JC
    Clin Obstet Gynaecol; 1980 Apr; 7(1):41-72. PubMed ID: 6155237
    [No Abstract]   [Full Text] [Related]  

  • 38. A consortium approach to molecular genetic services. Scottish Molecular Genetics Consortium.
    Brock DJ
    J Med Genet; 1990 Jan; 27(1):8-13. PubMed ID: 2308159
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Screening for disease: how far is too far?
    Lancet Neurol; 2005 Jan; 4(1):1. PubMed ID: 15620843
    [No Abstract]   [Full Text] [Related]  

  • 40. Genetic diagnosis of haemophilia and other inherited bleeding disorders.
    Peyvandi F; Jayandharan G; Chandy M; Srivastava A; Nakaya SM; Johnson MJ; Thompson AR; Goodeve A; Garagiola I; Lavoretano S; Menegatti M; Palla R; Spreafico M; Tagliabue L; Asselta R; Duga S; Mannucci PM
    Haemophilia; 2006 Jul; 12 Suppl 3():82-9. PubMed ID: 16684001
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.