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 *

128 related articles for article (PubMed ID: 4554519)

  • 1. Cell culture in inherited disease--with some notes on genetic heterogeneity.
    Bearn AG
    N Engl J Med; 1972 Apr; 286(14):764-7. PubMed ID: 4554519
    [No Abstract]   [Full Text] [Related]  

  • 2. Prenatal genetic diagnosis. 3.
    Milunsky A; Littlefield JW; Kanvfer JN; Kolodny EH; Shih VE; Atkins L
    N Engl J Med; 1970 Dec; 283(27):1498-504. PubMed ID: 4992307
    [No Abstract]   [Full Text] [Related]  

  • 3. [Prenatal diagnosis in hereditary metabolic diseases].
    Teller WM
    Dtsch Med Wochenschr; 1975 Aug; 100(33):1674-7. PubMed ID: 1098883
    [No Abstract]   [Full Text] [Related]  

  • 4. Prenatal diagnosis of inborn errors of metabolism.
    Mahoney MJ
    Clin Perinatol; 1979 Sep; 6(2):255-73. PubMed ID: 391465
    [No Abstract]   [Full Text] [Related]  

  • 5. Prenatal genetic diagnosis (second of three parts).
    Milunsky A; Littlefield JW; Kanfer JN; Kolodny EH; Shih VE; Atkins L
    N Engl J Med; 1970 Dec; 283(26):1441-7. PubMed ID: 4098222
    [No Abstract]   [Full Text] [Related]  

  • 6. Prenatal laboratory diagnosis of hereditary disorders. Amniocentesis and fibroblast tissue culture permit in utero diagnosis of hereditary metabolic disorders.
    Perl DP
    R I Med J; 1971 Oct; 54(10):509-12. PubMed ID: 4255433
    [No Abstract]   [Full Text] [Related]  

  • 7. [Possibilites and limitations in the prenatal diagnosis of genetic diseases].
    Galjaard H; Jahodova M; Niermijer MF
    Brux Med; 1972 Feb; 52(2):109-21. PubMed ID: 4258331
    [No Abstract]   [Full Text] [Related]  

  • 8. Deficiency of lysosomal acid phosphatase. A new familial metabolic disorder.
    Nadler HL; Egan TJ
    N Engl J Med; 1970 Feb; 282(6):302-7. PubMed ID: 5410815
    [No Abstract]   [Full Text] [Related]  

  • 9. [The genetic mechanisms of lysosomal enzymopathies].
    Poénaru L
    Endocrinologie; 1990; 28(3-4):211-4. PubMed ID: 2103976
    [No Abstract]   [Full Text] [Related]  

  • 10. [Use of DNA restriction fragment length polymorphisms in the diagnosis of genetically determined diseases].
    Zietkiewicz E; Latos-Bieleńska AM; Słomski R
    Pol Arch Med Wewn; 1985 Oct; 74(4):269-78. PubMed ID: 2907124
    [No Abstract]   [Full Text] [Related]  

  • 11. Newer procedures in the preconceptional, prenatal and early postnatal diagnosis of birth defects.
    Nadler HL
    Birth Defects Orig Artic Ser; 1970 May; 6(1):26-33. PubMed ID: 5522716
    [No Abstract]   [Full Text] [Related]  

  • 12. Genetic heterogeneity in inherited disease.
    Harris H
    J Clin Pathol Suppl (R Coll Pathol); 1974; 8():32-7. PubMed ID: 4536365
    [No Abstract]   [Full Text] [Related]  

  • 13. Gene derepression: possible applications to diagnosis and management of genetic disease.
    Benson PF
    Guys Hosp Rep; 1973; 122(1-2):91-108. PubMed ID: 4613623
    [No Abstract]   [Full Text] [Related]  

  • 14. Prenatal genetic diagnosis. I.
    Milunsky A; Littlefield JW; Kanfer JN; Kolodny EH; Shih VE; Atkins L
    N Engl J Med; 1970 Dec; 283(25):1370-81. PubMed ID: 4921307
    [No Abstract]   [Full Text] [Related]  

  • 15. [Prenatal diagnosis of congenital diseases of metabolism and of chromosomes alterations].
    Saggese R
    Pediatria (Napoli); 1979 Dec; 87(4):631-47. PubMed ID: 400008
    [No Abstract]   [Full Text] [Related]  

  • 16. [Enzyme deficiencies detected on cultured fibroblasts and amniotic cells. Application to prenatal diagnosis].
    Dreyfus JC; Poenaru L
    Ann Biol Clin (Paris); 1975; 33(6):465-72. PubMed ID: 818927
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The biochemical diagnosis of lysosomal storage diseases--a review of five years experience.
    Wallace IJ; McCusker CA; McCormick D
    Ir J Med Sci; 1990 Jul; 159(7):203-9. PubMed ID: 2283277
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Prenatal diagnosis of hereditary lysosomal diseases].
    Mirenburg TV; Aronovich EL; Lebedeva TV; Akhunov VS; Krasnopol'skaia KD
    Vopr Med Khim; 1988; 34(4):41-6. PubMed ID: 3143186
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Value and limitations of the tstudy of metachromasia on fibroblast culture in medical genetics].
    Guibaud P
    Pediatrie; 1970; 25(7):807-13. PubMed ID: 4098310
    [No Abstract]   [Full Text] [Related]  

  • 20. Genetic screening.
    Littlefield JW
    N Engl J Med; 1972 May; 286(21):1155-6. PubMed ID: 5019646
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.