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 *

73 related articles for article (PubMed ID: 1431211)

  • 1. Polymorphism of the human genome: markers for genetic linkage analyses in heritable diseases of the skin.
    Christiano AM; Uitto J
    J Invest Dermatol; 1992 Nov; 99(5):519-23. PubMed ID: 1431211
    [No Abstract]   [Full Text] [Related]  

  • 2. Genetic linkage mapping of heritable skin diseases: positional cloning versus the candidate gene approach.
    Uitto J
    J Invest Dermatol; 1994 Jun; 102(6):825-6. PubMed ID: 8006442
    [No Abstract]   [Full Text] [Related]  

  • 3. Intragenic TaqI restriction fragment length polymorphism (RFLP) in CICN4, between the loci for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects syndrome (MLS).
    Schnur RE; Wick PA
    Hum Genet; 1995 May; 95(5):594-5. PubMed ID: 7759088
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DNA-based prenatal diagnosis of heritable skin diseases.
    Christiano AM; Uitto J
    Arch Dermatol; 1993 Nov; 129(11):1455-9. PubMed ID: 7902070
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dermatoses in five related female carriers of X-linked chronic granulomatous disease.
    Garioch JJ; Sampson JR; Seywright M; Thomson J
    Br J Dermatol; 1989 Sep; 121(3):391-6. PubMed ID: 2803962
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dermatology and the human gene map.
    Moss C
    Br J Dermatol; 1991 Jan; 124(1):3-9. PubMed ID: 1993142
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A genetic linkage map of the human genome.
    Donis-Keller H; Green P; Helms C; Cartinhour S; Weiffenbach B; Stephens K; Keith TP; Bowden DW; Smith DR; Lander ES
    Cell; 1987 Oct; 51(2):319-37. PubMed ID: 3664638
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Two first cousins with spondyloepiphyseal dysplasia tarda (X linked recessive form), one also with poikiloderma atrophicans vasculare progressing to lymphocytic lymphoma.
    Branford WA; Beveridge GW; Wynne-Davies R
    J Med Genet; 1982 Jun; 19(3):210-3. PubMed ID: 6809944
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of a locus for dyschromatosis symmetrica hereditaria at chromosome 1q11-1q21.
    Zhang XJ; Gao M; Li M; Li M; Li CR; Cui Y; He PP; Xu SJ; Xiong XY; Wang ZX; Yuan WT; Yang S; Huang W
    J Invest Dermatol; 2003 May; 120(5):776-80. PubMed ID: 12713580
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Workshop on linkage analysis of hereditary skin diseases. University of California, San Francisco, April 22-24, 1990.
    Epstein E
    J Invest Dermatol; 1990 Dec; 95(6):727-8. PubMed ID: 1979081
    [No Abstract]   [Full Text] [Related]  

  • 11. [Prenatal diagnosis of cutaneous genetic diseases by the study of fetal DNA].
    Hovnanian A; De Prost Y
    Ann Dermatol Venereol; 1995; 122(4):173-85. PubMed ID: 8526412
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Heritable skin diseases with molecular defects in collagen or elastin.
    Uitto J; Shamban A
    Dermatol Clin; 1987 Jan; 5(1):63-84. PubMed ID: 3549080
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular pathology of the elastic fibers.
    Christiano AM; Uitto J
    J Invest Dermatol; 1994 Nov; 103(5 Suppl):53S-57S. PubMed ID: 7963685
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genome screen for quantitative trait loci underlying normal variation in femoral structure.
    Koller DL; Liu G; Econs MJ; Hui SL; Morin PA; Joslyn G; Rodriguez LA; Conneally PM; Christian JC; Johnston CC; Foroud T; Peacock M
    J Bone Miner Res; 2001 Jun; 16(6):985-91. PubMed ID: 11393795
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Linkage and association analyses of glaucoma related traits in a large pedigree from a Dutch genetically isolated population.
    Axenovich T; Zorkoltseva I; Belonogova N; van Koolwijk LM; Borodin P; Kirichenko A; Babenko V; Ramdas WD; Amin N; Despriet DD; Vingerling JR; Lemij HG; Oostra BA; Klaver CC; Aulchenko Y; van Duijn CM
    J Med Genet; 2011 Dec; 48(12):802-9. PubMed ID: 22058429
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Linkage analyses of multiple endocrine neoplasia, type 2 (MEN-2) with 23 classical genetic polymorphisms.
    Kruger SD; Gertner JM; Sparkes RS; Haedt LE; Crist M; Sparkes MC; Genel M; Kidd KK
    Hum Hered; 1986; 36(1):6-11. PubMed ID: 2868987
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic epidemiologic studies in the etiology of skin diseases.
    Amos CI; Bale SJ
    J Invest Dermatol; 1994 Jun; 102(6):46S-48S. PubMed ID: 8006436
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deletion 3q27----3qter associated with a new skin disorder?
    Happle R
    Hum Genet; 1990 Oct; 85(5):563-4. PubMed ID: 2227944
    [No Abstract]   [Full Text] [Related]  

  • 19. Dermatology and the new genetics--a plea.
    Epstein E
    J Am Acad Dermatol; 1990 Nov; 23(5 Pt 1):949-50. PubMed ID: 2254488
    [No Abstract]   [Full Text] [Related]  

  • 20. A genome-wide linkage scan for homocysteine levels suggests three regions of interest.
    Vermeulen SH; van der Vleuten GM; de Graaf J; Hermus AR; Blom HJ; Stalenhoef AF; den Heijer M
    J Thromb Haemost; 2006 Jun; 4(6):1303-7. PubMed ID: 16706975
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.