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 *

135 related articles for article (PubMed ID: 1440921)

  • 1. [Successes and prospects of molecular diagnosis of the most widespread inherited diseases].
    Baranov VS
    Tsitol Genet; 1992; 26(4):64-72. PubMed ID: 1440921
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular diagnosis of some common genetic diseases in Russia and the former USSR: present and future.
    Baranov VS
    J Med Genet; 1993 Feb; 30(2):141-6. PubMed ID: 8445619
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Molecular diagnosis of genetic diseases in Russia: current status and perspectives].
    Baranov VS
    Vestn Ross Akad Med Nauk; 1993; (9):27-31. PubMed ID: 7510179
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Molecular analysis of genetic diseases: an overview for clinicians.
    Javed AA; Huang Y; Bombard AT
    J Assoc Acad Minor Phys; 1995; 6(1):15-27. PubMed ID: 7858372
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis of inherited biochemical disorders. Current and future considerations.
    Legge M
    Chin Med J (Engl); 1984 Sep; 97(9):671-8. PubMed ID: 6443300
    [No Abstract]   [Full Text] [Related]  

  • 7. [Genomic structure and DNA diagnosis of hereditary monogenic diseases in the Volga-Ural region].
    Khidiiatova IM; Khusnutdinova EK
    Mol Biol (Mosk); 2004; 38(1):139-49. PubMed ID: 15042844
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic screening and testing by induced heteroduplex formation.
    Wood N; Bidwell J
    Electrophoresis; 1996 Jan; 17(1):247-54. PubMed ID: 8907549
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Current status of prenatal diagnosis by DNA analysis.
    Kazazian HH
    Birth Defects Orig Artic Ser; 1990; 26(3):210-6. PubMed ID: 2092848
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. [Early diagnosis of congenital metabolic diseases].
    Böhles H; Stehr K
    Fortschr Med; 1980 Jul; 98(25):955-7. PubMed ID: 7450633
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Prenatal diagnosis and screening of common genetic diseases in Hong Kong.
    Chan V; Chan TK; Tang M; Ghosh A
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():1-2. PubMed ID: 8629083
    [No Abstract]   [Full Text] [Related]  

  • 15. Cystic fibrosis, genetics, and DNA technology.
    Nugent CE
    Curr Opin Obstet Gynecol; 1991 Apr; 3(2):235-41. PubMed ID: 1912355
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Strategies and logistical requirements for efficient testing in genetic disease.
    Jackson-Cook C; Pandya A
    Clin Lab Med; 1995 Dec; 15(4):839-57. PubMed ID: 8838226
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Screening for genetic diseases with molecular probes].
    Ann Biol Clin (Paris); 1985; 43(4):355-68. PubMed ID: 4091299
    [No Abstract]   [Full Text] [Related]  

  • 18. [Recent progress in the diagnosis and treatment of genetic diseases].
    Koller PC
    Recenti Prog Med; 1976 Oct; 61(4):557-70. PubMed ID: 828969
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. Uses of dinucleotide/trinucleotide repeats in the diagnosis of genetic diseases.
    Chan V; Yip B; Chan TP; Chan TK
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():179-81. PubMed ID: 8629102
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.