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 *

120 related articles for article (PubMed ID: 6879807)

  • 1. [Preventive fetal chromosome examinations in Denmark. Report from the Central Cytogenetic Register].
    Ugeskr Laeger; 1983 Jun; 145(23):1760-2. PubMed ID: 6879807
    [No Abstract]   [Full Text] [Related]  

  • 2. [Pregnancy wastage and prenatal diagnosis].
    Grünfeld B; van der Hagen CB
    Tidsskr Nor Laegeforen; 1985 May; 105(15):1079-81. PubMed ID: 4012713
    [No Abstract]   [Full Text] [Related]  

  • 3. Chromosome examination of 20,222 newborn children: results from a 7.5-year study in Arhus, Denmark.
    Nielsen J; Wohlert M; Faaborg-Andersen J; Eriksen G; Hansen KB; Hvidman L; Krag-Olsen B; Moulvad I; Videbech P
    Birth Defects Orig Artic Ser; 1986; 22(3):209-19. PubMed ID: 3814777
    [No Abstract]   [Full Text] [Related]  

  • 4. Prenatal diagnosis and multiple gestation.
    Meier PR; Saunders B
    Birth Defects Orig Artic Ser; 1982; 18(3 Pt A):121-4. PubMed ID: 7126784
    [No Abstract]   [Full Text] [Related]  

  • 5. [Prenatal cytogenetic diagnosis at the Institute for Maternal and Child Care (results of 2700 successful examinations in the 2d trimester of pregnancy)].
    Subrt I; Benesová O; Stirská K; Zwinger A
    Cesk Gynekol; 1989 Dec; 54(10):768-71. PubMed ID: 2630043
    [No Abstract]   [Full Text] [Related]  

  • 6. Prenatal genetic diagnosis.
    Jones WR
    Med J Aust; 1985 Jul; 143(2):55. PubMed ID: 4021871
    [No Abstract]   [Full Text] [Related]  

  • 7. [Diagnosis of chromosome abnormalities in Denmark].
    Nielsen J
    Ugeskr Laeger; 1978 Oct; 140(41):2495-99. PubMed ID: 695100
    [No Abstract]   [Full Text] [Related]  

  • 8. [Antenatal diagnosis. 601 chromosome examinations (author's transl)].
    Taillemite JL; Le Porrier N; Joye N; Delubac D; Colau JC; Van den Akker J; Portnoi MF; Roux C
    J Gynecol Obstet Biol Reprod (Paris); 1981; 10(1):33-8. PubMed ID: 7252086
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Prenatal screening for abnormalities and chromosomal disorders].
    Brandt NJ; Skovby F
    Ugeskr Laeger; 1996 Feb; 158(9):1197. PubMed ID: 8644422
    [No Abstract]   [Full Text] [Related]  

  • 10. Genetic counseling after unexpected cytogenetic findings on prenatal diagnosis.
    Kelly TE
    Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():183-5. PubMed ID: 11400765
    [No Abstract]   [Full Text] [Related]  

  • 11. Cytogenetic analysis in prenatal diagnosis.
    Schonberg SA
    West J Med; 1993 Sep; 159(3):360-5. PubMed ID: 8236978
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of a 5/15 translocation with 5p and proximal 5q trisomy. Cytogenetic and phenotypic findings.
    Crowder WE; Yeast JD; Falk RE
    Birth Defects Orig Artic Ser; 1982; 18(3 Pt A):143-51. PubMed ID: 7126787
    [No Abstract]   [Full Text] [Related]  

  • 13. [The prenatal cytogenetic diagnosis of fetal chromosomal pathology in women in a high-risk group].
    Nikitchyna TV; Baryliak IR; Hordiienko IIu
    Tsitol Genet; 1996; 30(5):22-6. PubMed ID: 9026986
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis: chromosome disorders.
    Antley RM; Melin JR
    J Indiana State Med Assoc; 1982 Apr; 75(4):262-3. PubMed ID: 7086160
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. Cytogenetic analysis of fetal chondrocytes: a comparative study.
    Gelman-Kohan Z; Rosensaft J; Ben-Hur H; Haber A; Chemke J
    Prenat Diagn; 1996 Feb; 16(2):165-8. PubMed ID: 8650128
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal exclusion of segmental trisomy in familial chromosome 21 pericentric inversion by fluorescence in situ hybridization.
    Tardy EP; Tóth A; Kosztolányi G
    Prenat Diagn; 1997 Sep; 17(9):871-3. PubMed ID: 9316133
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Partial trisomy 13 for the distal long arm and its prenatal diagnosis].
    Zolotukhina TV; Rozovskiĭ IS; Bartseva OB; Vakhlamova IV; Bubnova NI
    Genetika; 1982 Nov; 18(11):1899-905. PubMed ID: 6891355
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Prenatal diagnosis in Scandinavia].
    Brøndum-Nielsen K; Nørgaard-Pedersen B
    Nord Med; 1993; 108(6-7):189-92. PubMed ID: 8321644
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.