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 *

157 related articles for article (PubMed ID: 4464238)

  • 1. Detection of heterozygotes for aspartylglucosaminuria (AGU) in cultured fibroblasts.
    Aula P; Autio S; Raivio K; Näntö V
    Humangenetik; 1974; 25(4):307-14. PubMed ID: 4464238
    [No Abstract]   [Full Text] [Related]  

  • 2. Prenatal diagnosis and fetal pathology of aspartylglucosaminuria.
    Aula P; Rapola J; von Koskull H; Ammälä P
    Am J Med Genet; 1984 Oct; 19(2):359-67. PubMed ID: 6507482
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cultured skin fibroblasts in disorders of glycoprotein catabolism and I-cell disease.
    Autio S; Aula P; Näntö V
    Dev Med Child Neurol; 1974 Jun; 16(3):376-8. PubMed ID: 4407630
    [No Abstract]   [Full Text] [Related]  

  • 4. [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]  

  • 5. First-trimester prenatal diagnosis of aspartylglucosaminuria.
    Aula P; Mattila K; Piiroinen O; Ammälä P; Von Koskull H
    Prenat Diagn; 1989 Sep; 9(9):617-20. PubMed ID: 2798347
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Infantile metachromatic leukodystrophy. Confirmation of a prenatal diagnosis.
    Leroy JG; Van Elsen AF; Martin JJ; Dumon JE; Hulet AE; Okada S; Navarro C
    N Engl J Med; 1973 Jun; 288(26):1365-9. PubMed ID: 4707419
    [No Abstract]   [Full Text] [Related]  

  • 7. Electrophoretic detection of hexosaminidase I in amniotic fluid.
    Wysocki SJ; Hähnel R
    Clin Chim Acta; 1976 Mar; 67(2):219-20. PubMed ID: 942889
    [No Abstract]   [Full Text] [Related]  

  • 8. Aspartylglycosaminuria, urinary excretion of aspartylglycosamines related to mental retardation.
    Borud O; Torp KH; Dahl T
    Monogr Hum Genet; 1978; 10():23-6. PubMed ID: 723900
    [No Abstract]   [Full Text] [Related]  

  • 9. Globoid cell (Krabbe's) leukodystrophy: heterozygote detection in cultured skin fibroblasts.
    Farrell DF; Percy AK; Kaback MM; McKhann GM
    Am J Hum Genet; 1973 Nov; 25(6):604-9. PubMed ID: 4773478
    [No Abstract]   [Full Text] [Related]  

  • 10. Rapid tissue culture and microbiochemical methods for analyzing colonially grown fibroblasts from normal, Lesch-Nyhan and Tay-Sachs patients and amniotic fluid cells.
    Richardson BJ; Cox DM
    Clin Genet; 1973; 4(5):376-80. PubMed ID: 4751308
    [No Abstract]   [Full Text] [Related]  

  • 11. Aspartylglucosaminuria: deficiency of aspartylglucosaminidase in cultured fibroblasts of patients and their heterozygous parents.
    Aula P; Näntö V; Laipio ML; Autio S
    Clin Genet; 1973; 4(3):297-300. PubMed ID: 4765214
    [No Abstract]   [Full Text] [Related]  

  • 12. Lysosomal enzymes of amniotic fluid in relation to gestational age.
    Butterworth J; Broadhead DM; Sutherland GR; Bain AD
    Am J Obstet Gynecol; 1974 Jul; 119(6):821-8. PubMed ID: 4841183
    [No Abstract]   [Full Text] [Related]  

  • 13. Aspartylglucosaminuria in the United States.
    Hreidarsson S; Thomas GH; Valle DL; Stevenson RE; Taylor H; McCarty J; Coker SB; Green WR
    Clin Genet; 1983 Jun; 23(6):427-35. PubMed ID: 6883788
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Tissue culture and antenatal detection of molecular diseases.
    Nadler HL
    Biochimie; 1972; 54(5):677-82. PubMed ID: 4654164
    [No Abstract]   [Full Text] [Related]  

  • 15. The use of quantiatative cytochemical analyses in rapid prenatal detection and somatic cell genetic studies of metabolic diseases.
    Galjaard H; Hoogeveen A; Keijzer W; De Wit-Verbeek E; Vlek-Noot C
    Histochem J; 1974 Sep; 6(5):491-509. PubMed ID: 4214804
    [No Abstract]   [Full Text] [Related]  

  • 16. Elevated activity of lysosomal enzymes in amniotic fluid of a fetus with mucolipidosis II (I-cell disease).
    Huijing F; Warren RJ; McLeod AG
    Clin Chim Acta; 1973 Mar; 44(3):453-5. PubMed ID: 4694487
    [No Abstract]   [Full Text] [Related]  

  • 17. Sanfilippo syndrome: profound deficiency of alpha-acetylglucosaminidase activity in organs and skin fibroblasts from type-B patients.
    O'Brien JS
    Proc Natl Acad Sci U S A; 1972 Jul; 69(7):1720-2. PubMed ID: 4261742
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The prenatal diagnosis of inborn errors of metabolism.
    Milunsky A; Littlefield JW
    Annu Rev Med; 1972; 23():57-76. PubMed ID: 4264784
    [No Abstract]   [Full Text] [Related]  

  • 19. Intrauterine diagnosis: comparative enzymology of cells cultivated from maternal skin, fetal skin, and amniotic fluid cells.
    Kaback MM; Leonard CO; Parmley TH
    Pediatr Res; 1971 Aug; 5(8):366-71. PubMed ID: 5146085
    [No Abstract]   [Full Text] [Related]  

  • 20. Detection of aspartylglycosaminuria by gas--liquid chromatography.
    Maury CP
    Clin Chem; 1981 Dec; 27(12):2058-60. PubMed ID: 7307258
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.