BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 9835018)

  • 1. Genatlas database, genes and development defects.
    Frézal J
    C R Acad Sci III; 1998 Oct; 321(10):805-17. PubMed ID: 9835018
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Body plan genes and human malformation.
    Boncinelli E; Mallamaci A; Broccoli V
    Adv Genet; 1998; 38():1-29. PubMed ID: 9677704
    [No Abstract]   [Full Text] [Related]  

  • 3. Homeobox genes and disease.
    Boncinelli E
    Curr Opin Genet Dev; 1997 Jun; 7(3):331-7. PubMed ID: 9229108
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Are abnormalities of human organizational genes responsible for causing birth defects?
    Bamforth JS
    Reprod Toxicol; 1994; 8(6):455-9. PubMed ID: 7881197
    [No Abstract]   [Full Text] [Related]  

  • 5. [Genetic control of fetal development. Abnormalities in Drosophila yield new clues].
    Ringertz N
    Lakartidningen; 1993 Jun; 90(26-27):2444-6. PubMed ID: 8100287
    [No Abstract]   [Full Text] [Related]  

  • 6. Congenital abnormalities of body patterning: embryology revisited.
    Goodman FR
    Lancet; 2003 Aug; 362(9384):651-62. PubMed ID: 12944067
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [The homeo box--a genetic key to fetal development].
    Njølstad PR; Molven A
    Tidsskr Nor Laegeforen; 1993 May; 113(12):1475-9. PubMed ID: 8101395
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The large-scale Munich ENU-mouse-mutagenesis screen.
    Soewarto D; Fella C; Teubner A; Rathkolb B; Pargent W; Heffner S; Marschall S; Wolf E; Balling R; Hrabé de Angelis M
    Mamm Genome; 2000 Jul; 11(7):507-10. PubMed ID: 10886013
    [No Abstract]   [Full Text] [Related]  

  • 9. Human genetics: past, present, and future, with special reference to major trends in Japan.
    Yanase T
    Jpn J Hum Genet; 1997 Jun; 42(2):265-316. PubMed ID: 9290255
    [No Abstract]   [Full Text] [Related]  

  • 10. Genetic causes of abnormal fetal development and inherited disease.
    Eppink H
    JOGN Nurs; 1977; 6(5):14-22. PubMed ID: 333156
    [No Abstract]   [Full Text] [Related]  

  • 11. Finding the genes that direct mammalian development : ENU mutagenesis in the mouse.
    Anderson KV
    Trends Genet; 2000 Mar; 16(3):99-102. PubMed ID: 10689347
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Homeobox genes: molecular link between congenital anomalies and cancer.
    Anbazhagan R; Raman V
    Eur J Cancer; 1997 Apr; 33(4):635-7. PubMed ID: 9274447
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Human HOX gene disorders.
    Quinonez SC; Innis JW
    Mol Genet Metab; 2014 Jan; 111(1):4-15. PubMed ID: 24239177
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Synthesizing embryology and human genetics: paradigms regained.
    Gilbert SF
    Am J Hum Genet; 1992 Jul; 51(1):211-5. PubMed ID: 1351698
    [No Abstract]   [Full Text] [Related]  

  • 15. Scoring a technical knockout in mice.
    Travis J
    Science; 1992 Jun; 256(5062):1392-4. PubMed ID: 1351316
    [No Abstract]   [Full Text] [Related]  

  • 16. Fetal phenotypic analysis.
    Elejalde BR; de Elejalde MM
    Indian J Pediatr; 1986; 53(4):477-88. PubMed ID: 3542816
    [No Abstract]   [Full Text] [Related]  

  • 17. [Developmental disorders of man. Part 2].
    Opitz JM
    Monatsschr Kinderheilkd; 1992 May; 140(5):264-72. PubMed ID: 1352038
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The human gene mutation database.
    Krawczak M; Cooper DN
    Trends Genet; 1997 Mar; 13(3):121-2. PubMed ID: 9066272
    [No Abstract]   [Full Text] [Related]  

  • 19. Contiguous gene syndromes: a component of recognizable syndromes.
    Schmickel RD
    J Pediatr; 1986 Aug; 109(2):231-41. PubMed ID: 3016222
    [No Abstract]   [Full Text] [Related]  

  • 20. Bridging the gap between molecular genetics and metabolic medicine: access to genetic information.
    Aymé S
    Eur J Pediatr; 2000 Dec; 159 Suppl 3():S183-5. PubMed ID: 11216896
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.