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 *

136 related articles for article (PubMed ID: 153809)

  • 21. Hunter syndrome in Jews in Israel: further evidence for prenatal selection favoring the Hunter allele.
    Zlotogora J; Schaap T; Zeigler M; Bach G
    Hum Genet; 1991 Mar; 86(5):531-3. PubMed ID: 1901828
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prenatal diagnosis of mucolipidosis II (I-cell disease).
    Gehler J; Cantz M; Stoeckenius M; Spranger J
    Eur J Pediatr; 1976 Jun; 122(3):201-6. PubMed ID: 819273
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prenatal diagnosis of Hunter syndrome using fetal plasma.
    Lissens W; Van Lierde M; Decaluwe J; Foulon W; Evrard P; Van Hoof F; Freund M; Liebaers I
    Prenat Diagn; 1988 Jan; 8(1):59-62. PubMed ID: 3125535
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Present status of amniocentesis in intrauterine diagnosis of genetic defects.
    Nadler HL; Gerbie A
    Obstet Gynecol; 1971 Nov; 38(5):789-99. PubMed ID: 5114231
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Prenatal diagnosis of Hunter's disease].
    Bolodár A; Török O; Horváth K; Németi M; Szabó M; Papp Z
    Orv Hetil; 1990 May; 131(19):1025-7. PubMed ID: 2111903
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Reliability of the use of fructose 1-phosphate to detect Hunter cells in fibroblast-cultures of obligate carriers of the Hunter syndrome.
    Tønnesen T; Güttler F; Lykkelund C
    Hum Genet; 1983; 64(4):371-5. PubMed ID: 6225723
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prenatal diagnosis of genetic disorders.
    Niermeijer MF; Sachs ES; Jahodova M; Tichelaar-Klepper C; Kleijer WJ; Galjaard H
    J Med Genet; 1976 Jun; 13(3):182-94. PubMed ID: 58990
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].
    Zhang YP; Wu JP; Li XT; Lei CX; Xu JZ; Yin M
    Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):644-8. PubMed ID: 22176986
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal diagnosis of X-linked adrenoleukodystrophy combining biochemical, immunocytochemical and DNA analyses.
    Maier EM; Roscher AA; Kammerer S; Mehnert K; Conzelmann E; Holzinger A
    Prenat Diagn; 1999 Apr; 19(4):364-8. PubMed ID: 10327143
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Diagnosis of Hunter's syndrome carriers; radioactive sulphate incorporation into fibroblasts in the presence or fructose 1-phosphate.
    Tønnesen T; Lykkelund C; Güttler F
    Hum Genet; 1982; 60(2):167-71. PubMed ID: 6210620
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Hunter syndrome among Ashkenazi Jews in Israel; evidence for prenatal selection favoring the Hunter allele.
    Zlotogora J; Schaap T; Zeigler M; Bach G
    Hum Genet; 1985; 71(4):329-32. PubMed ID: 3935563
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Reliability of the Booth-Nadler technique for the detection of Hunter heterozygotes.
    Donnelly PV; Di Ferrante N
    Pediatrics; 1975 Sep; 56(3):429-33. PubMed ID: 808791
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Correct prenatal diagnosis of a Hurler fetus where amniotic fluid cell cultures were of maternal origin.
    Mossman J; Patrick AD; Fensom AH; Tansley LR; Benson PF; Der Kaloustian VM; Dudin G
    Prenat Diagn; 1981 Apr; 1(2):121-4. PubMed ID: 6810332
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Preparation, culture, and analysis of amniotic fluid samples.
    Miron PM
    Curr Protoc Hum Genet; 2012 Jul; Chapter 8():Unit8.4. PubMed ID: 22786614
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prenatal diagnosis of mucopolysaccharidosis by two-dimensional electrophoresis of amniotic fluid glycosaminoglycans.
    Mossman J; Patrick AD
    Prenat Diagn; 1982 Jul; 2(3):169-76. PubMed ID: 6815629
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Prenatal diagnosis of genetic defects from the amniotic fluid. Report of experiences].
    Körner H; Halle H; Wagenknecht C
    Zentralbl Gynakol; 1977; 99(12):725-34. PubMed ID: 70907
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular genetic characterization and prenatal diagnosis in a family with Hunter disease.
    Grosso M; Balzano N; Rippa E; Villani GR; Salvatore F; Izzo P; di Natale P
    Biochem Mol Biol Int; 1995 May; 35(6):1261-7. PubMed ID: 7492964
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Mutation analysis of mucopolysaccharidosis type II and prenatal diagnosis].
    Liu N; Shi H; Kong X; Wu Q; Jiang M
    Zhonghua Fu Chan Ke Za Zhi; 2014 Jun; 49(6):410-3. PubMed ID: 25169630
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The prenatal diagnosis of adrenoleukodystrophy. Demonstration of increased hexacosanoic acid levels in cultured amniocytes and fetal adrenal gland.
    Moser HW; Moser AB; Powers JM; Nitowsky HM; Schaumburg HH; Norum RA; Migeon BR
    Pediatr Res; 1982 Mar; 16(3):172-5. PubMed ID: 7063272
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prenatal diagnosis and fetal pathology of I-cell disease (mucolipidosis type II).
    Aula P; Rapola J; Autio S; Raivio K; Karjalainen O
    J Pediatr; 1975 Aug; 87(2):221-6. PubMed ID: 168339
    [TBL] [Abstract][Full Text] [Related]  

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