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 *

153 related articles for article (PubMed ID: 7224004)

  • 1. [Prenatal fetal karyotype diagnosis in phenotypically healthy women with balanced chromosome rearrangements].
    Rozovskiĭ IS; Zolotukhina TV; Butomo IV
    Akush Ginekol (Mosk); 1981 Jan; (1):15-8. PubMed ID: 7224004
    [No Abstract]   [Full Text] [Related]  

  • 2. Chromosome analysis of fetuses in risk pregnancies.
    Philip J; Bang J; Hahnemann N; Mikkelsen M; Niebuhr E; Rebbe H; Weber J
    Acta Obstet Gynecol Scand Suppl; 1974; 29():9-14. PubMed ID: 4276258
    [No Abstract]   [Full Text] [Related]  

  • 3. Abnormal chromosome 18 in prenatal diagnosis with holoprosencephaly.
    de Pater JM; Scheres JM; Brons J
    Prenat Diagn; 1997 Sep; 17(9):887-8. PubMed ID: 9316141
    [No Abstract]   [Full Text] [Related]  

  • 4. Prenatal cytogenetic diagnosis in 1500 mid-trimester amniocenteses.
    Yang ML; Leung WY; Yang ZL; Hsu I; Chen LJ; Lin WY; Ng HT
    Zhonghua Yi Xue Za Zhi (Taipei); 1988 Oct; 42(4):275-80. PubMed ID: 3242765
    [No Abstract]   [Full Text] [Related]  

  • 5. Prenatal diagnosis of a congenital anomaly of isochromosome 18q--a case report.
    Shyu SK; Yang ML; Ng HT; Hsu I; Wang JS; Ho DM
    Zhonghua Yi Xue Za Zhi (Taipei); 1988 May; 41(5):383-8. PubMed ID: 3219651
    [No Abstract]   [Full Text] [Related]  

  • 6. [A case of fetal triploidy associated with low maternal serum alpha-fetoprotein].
    Hamada H; Koresawa M; Kubo T
    Nihon Sanka Fujinka Gakkai Zasshi; 1991 Jul; 43(7):799-802. PubMed ID: 1716294
    [No Abstract]   [Full Text] [Related]  

  • 7. [Chromosome rearrangements (balanced translocations) and their importance in perinatal pathology].
    Khodzhaeva ZS
    Akush Ginekol (Mosk); 1981 Jan; (1):9-12. PubMed ID: 7013527
    [No Abstract]   [Full Text] [Related]  

  • 8. Prenatal diagnosis of a mosaic extra structurally abnormal chromosome by spectral karyotyping.
    Ning Y; Laundon CH; Schröck E; Buchanan P; Ried T
    Prenat Diagn; 1999 May; 19(5):480-2. PubMed ID: 10360520
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A case of mosaicism involving an unstable 13/14 Robertsonian translocation.
    Wells S; Gregson N; Porter RJ
    Prenat Diagn; 1991 Nov; 11(11):875-80. PubMed ID: 1754558
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Ways to improve prenatal diagnosis of chromosome abnormalities and congenital defects of fetal development].
    Bakharev VA; Polesterov IuA; Gavrilova IuV
    Akush Ginekol (Mosk); 1990 Jan; (1):16-8. PubMed ID: 1693812
    [No Abstract]   [Full Text] [Related]  

  • 11. Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding.
    Jacobs PA; Browne C; Gregson N; Joyce C; White H
    J Med Genet; 1992 Feb; 29(2):103-8. PubMed ID: 1613759
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
    DuPont BR; Huff RW; Ridgway LE; Stratton RF; Moore CM
    Am J Med Genet; 1994 Mar; 50(1):21-7. PubMed ID: 8160748
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rapid DNA quantification in the prenatal diagnosis of fetal triploidy.
    Thilaganathan B; Makrydimas G; Nicolaides KH
    Br J Obstet Gynaecol; 1993 Jan; 100(1):92-3. PubMed ID: 8427846
    [No Abstract]   [Full Text] [Related]  

  • 14. Fetal chromosome abnormalities detected in mid pregnancy.
    Craft I; Hill L; Chitham RG
    Br J Clin Pract; 1976 May; 30(5):102-3, 106. PubMed ID: 952699
    [No Abstract]   [Full Text] [Related]  

  • 15. [Chorionic villi sampling and prenatal diagnosis].
    Horovitz J; Saura R; Spalova I
    Rev Fr Gynecol Obstet; 1992 Apr; 87(4):183-7. PubMed ID: 1615271
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Laboratory research on problems of fetal and early life.
    Weiss DL
    Ann Clin Lab Sci; 1982; 12(6):500-7. PubMed ID: 6758677
    [No Abstract]   [Full Text] [Related]  

  • 17. Inv dup(15) supernumerary marker chromosomes.
    Webb T
    J Med Genet; 1994 Aug; 31(8):585-94. PubMed ID: 7815414
    [No Abstract]   [Full Text] [Related]  

  • 18. Confirmation of the chromosome 8p23.1 euchromatic duplication as a variant with no clinical manifestations.
    O'Malley DP; Storto PD
    Prenat Diagn; 1999 Feb; 19(2):183-4. PubMed ID: 10215083
    [No Abstract]   [Full Text] [Related]  

  • 19. [Pay more attention to cytogenetics in prenatal diagnosis].
    Bian XM; Qi QW
    Zhonghua Fu Chan Ke Za Zhi; 2013 Nov; 48(11):801-4. PubMed ID: 24444553
    [No Abstract]   [Full Text] [Related]  

  • 20. Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p.
    De Pater JM; Van Tintelen JP; Stigter R; Brouwers HA; Scheres JM
    Genet Couns; 2000; 11(3):241-7. PubMed ID: 11043432
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.