BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 2572536)

  • 1. Haplotype frequencies of the collagen type-I genes in the Italian population.
    Mottes M; Cugola L; Pignatti PF
    Hum Genet; 1989 Nov; 83(4):369-72. PubMed ID: 2572536
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families.
    Mottes M; Sangalli A; Pignatti PF
    Am J Med Genet; 1993 Jan; 45(2):217-22. PubMed ID: 8096115
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Strategy for prenatal diagnosis of osteogenesis imperfecta by linkage analysis to the type I collagen loci COL1A1 and COL1A2.
    Benušienė E; Kučinskas V
    Med Sci Monit; 2000; 6(2):217-26. PubMed ID: 11208313
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Studies on four restriction fragment length polymorphisms of the type I collagen genes in two Italian populations.
    Pepe G; Muglia M; Brancati C; Modiano G
    Hum Hered; 1990; 40(6):368-80. PubMed ID: 1982109
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Segregation analysis of dominant osteogenesis imperfecta in Italy.
    Mottes M; Cugola L; Cappello N; Pignatti PF
    J Med Genet; 1990 Jun; 27(6):367-70. PubMed ID: 1972760
    [TBL] [Abstract][Full Text] [Related]  

  • 6. COL1A2 gene (alpha 2 gene of type I collagen) at the haplotype level as a new valuable anthropogenetic marker: a study on Sardinians.
    Pepe G; Bue C; Orlandi P; Ena F; Meloni T; Modiano G
    Hum Biol; 1994 Aug; 66(4):613-23. PubMed ID: 7916321
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Allele and haplotype frequency distribution of the EcoRI, RsaI, and MspI COL1A2 RFLPs among various human populations.
    Pepe G; Rickards O; Jodice C; Modiano G
    Hum Biol; 1995 Dec; 67(6):905-20. PubMed ID: 8543299
    [TBL] [Abstract][Full Text] [Related]  

  • 8. EcoRI, RsaI, and MspI RFLPs of the COL1A2 gene (type I collagen) in the Cayapa, a Native American population of Ecuador.
    Pepe G; Rickards O; Bué C; Martinez-Labarga C; Tartaglia M; De Stefano GF
    Hum Biol; 1994 Dec; 66(6):979-89. PubMed ID: 7835877
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Osteogenesis imperfecta type III: mutations in the type I collagen structural genes, COL1A1 and COL1A2, are not necessarily responsible.
    Wallis GA; Sykes B; Byers PH; Mathew CG; Viljoen D; Beighton P
    J Med Genet; 1993 Jun; 30(6):492-6. PubMed ID: 8100856
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2.
    Sykes B; Ogilvie D; Wordsworth P; Wallis G; Mathew C; Beighton P; Nicholls A; Pope FM; Thompson E; Tsipouras P
    Am J Hum Genet; 1990 Feb; 46(2):293-307. PubMed ID: 1967900
    [TBL] [Abstract][Full Text] [Related]  

  • 11. COL1A2 (type I collagen) polymorphisms in the Colorado Indians of Ecuador.
    Babalini C; Tarsi T; Martínez-Labarga C; Scano G; Pepe G; De Stefano GF; Rickards O
    Ann Hum Biol; 2005; 32(5):666-78. PubMed ID: 16316921
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Variability and distribution of COL1A2 (type I collagen) polymorphisms in the central-eastern Mediterranean Basin.
    Scorrano G; Lelli R; Martínez-Labarga C; Scano G; Contini I; Hafez HS; Rudan P; Rickards O
    Ann Hum Biol; 2016; 43(1):73-7. PubMed ID: 26065693
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal prediction of osteogenesis imperfecta (OI type IV): exclusion of inheritance using a collagen gene probe.
    Tsipouras P; Schwartz RC; Goldberg JD; Berkowitz RL; Ramirez F
    J Med Genet; 1987 Jul; 24(7):406-9. PubMed ID: 2886666
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Three unrelated individuals with perinatally lethal osteogenesis imperfecta resulting from identical Gly502Ser substitutions in the alpha 2-chain of type I collagen.
    Rose NJ; Mackay K; De Paepe A; Steinmann B; Punnett HH; Dalgleish R
    Hum Genet; 1994 Nov; 94(5):497-503. PubMed ID: 7959683
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical variability of osteogenesis imperfecta linked to COL1A2 and associated with a structural defect in the type I collagen molecule.
    Superti-Furga A; Pistone F; Romano C; Steinmann B
    J Med Genet; 1989 Jun; 26(6):358-62. PubMed ID: 2567784
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Homozygous osteogenesis imperfecta unlinked to collagen I genes.
    Aitchison K; Ogilvie D; Honeyman M; Thompson E; Sykes B
    Hum Genet; 1988 Mar; 78(3):233-6. PubMed ID: 2894346
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Restriction fragment length polymorphisms of three collagen genes in Russians and Buryats.
    Sokolov BP; Dzemelinski VV; Kalinin VN
    Hum Hered; 1991; 41(1):57-60. PubMed ID: 1675622
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A highly polymorphic (ACT)n VNTR (variable nucleotide of tandem repeats) locus inside intron 12 of COL1A2, one of the two genes involved in dominant osteogenesis imperfecta.
    Pepe G
    Hum Mutat; 1993; 2(4):300-5. PubMed ID: 8104634
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Osteogenesis imperfecta type I is commonly due to a COL1A1 null allele of type I collagen.
    Willing MC; Pruchno CJ; Atkinson M; Byers PH
    Am J Hum Genet; 1992 Sep; 51(3):508-15. PubMed ID: 1353940
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutational spectrum of type I collagen genes in Korean patients with osteogenesis imperfecta.
    Lee KS; Song HR; Cho TJ; Kim HJ; Lee TM; Jin HS; Park HY; Kang S; Jung SC; Koo SK
    Hum Mutat; 2006 Jun; 27(6):599. PubMed ID: 16705691
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.