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 *

119 related articles for article (PubMed ID: 4509085)

  • 1. [Dental survey in Hailuoto. V. Torus mandibularis: incidence and some viewpoints connected with inheritance].
    Alvesalo L; Kari M
    Proc Finn Dent Soc; 1972; 68(6):307-14. PubMed ID: 4509085
    [No Abstract]   [Full Text] [Related]  

  • 2. [Data on torus mandibularis].
    Tanrykuliev P
    Stomatologiia (Mosk); 1972; 51(5):95-6. PubMed ID: 4506483
    [No Abstract]   [Full Text] [Related]  

  • 3. Torus mandibularis in an Alaskan Eskimo population.
    Mayhall JT; Dahlberg AA; Owen DG
    Am J Phys Anthropol; 1970 Jul; 33(1):57-60. PubMed ID: 5431487
    [No Abstract]   [Full Text] [Related]  

  • 4. A study of torus palatinus and torus mandibularis in Pre-Columbian Peruvians.
    Sawyer DR; Allison MJ; Elzay RP; Pezzia A
    Am J Phys Anthropol; 1979 May; 50(4):525-6. PubMed ID: 380359
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic approaches to the nosology of nervous system defects.
    Becker PE
    Birth Defects Orig Artic Ser; 1971 Feb; 7(1):10-22. PubMed ID: 5173354
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The prevalence of torus palatinus.
    King DR; Moore GE
    J Oral Med; 1971 Dec; 26(3):113-5. PubMed ID: 5288703
    [No Abstract]   [Full Text] [Related]  

  • 7. Prevalence of torus palatinus and torus mandibularis in five Asian populations.
    Ohno N; Sakai T; Mizutani T
    Aichi Gakuin Dent Sci; 1988; 1():1-8. PubMed ID: 3270475
    [No Abstract]   [Full Text] [Related]  

  • 8. X-linked mental retardation and verbal disability.
    Lehrke RG
    Birth Defects Orig Artic Ser; 1974; 10(1):1-100. PubMed ID: 4458821
    [No Abstract]   [Full Text] [Related]  

  • 9. Hereditary degeneration of the optic nerve (hereditary optic atrophy).
    Francois J
    Int Ophthalmol Clin; 1968; 8(4):999-1054. PubMed ID: 4907160
    [No Abstract]   [Full Text] [Related]  

  • 10. Prevalence of torus palatinus and torus mandibularis in 1000 patients.
    Shah DS; Sanghavi SJ; Chawda JD; Shah RM
    Indian J Dent Res; 1992; 3(4):107-10. PubMed ID: 1344979
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial epidermodysplasia verruciformis of Lewandowsky and Lutz.
    Rajagopalan K; Bahru J; Loo DS; Tay CH; Chin KN; Tan KK
    Arch Dermatol; 1972 Jan; 105(1):73-8. PubMed ID: 5009624
    [No Abstract]   [Full Text] [Related]  

  • 12. [X-chromosomal recessive retinoschisis].
    Eriksson AW; Forsius H; Vainio-Mattila B
    Duodecim; 1972; 88(1):43-51. PubMed ID: 5013576
    [No Abstract]   [Full Text] [Related]  

  • 13. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E; Palmieri A; Bertola A; Bellini C
    Genet Couns; 1995; 6(4):309-12. PubMed ID: 8775417
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The influence of sex-chromosome genes on tooth size in man. A genetic and quantitative study.
    Alvesalo L
    Suom Hammaslaak Toim; 1971; 67(1):3-54. PubMed ID: 5280409
    [No Abstract]   [Full Text] [Related]  

  • 15. [The stomato-anthropological study of the population from the Bicaz area].
    Firu P; Dumitrescu S; Stoica L
    Stomatologia (Bucur); 1974; 21(2):37-114. PubMed ID: 4522682
    [No Abstract]   [Full Text] [Related]  

  • 16. High incidence of autosomal recessive nonsyndromal congenital retinal nonattachment (NCRNA) in an Iranian founding population.
    Ghiasvand NM; Shirzad E; Naghavi M; Vaez Mahdavi MR
    Am J Med Genet; 1998 Jul; 78(3):226-32. PubMed ID: 9677055
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Juvenile retinoschisis].
    Remky H; Hildebrandt P
    Klin Monbl Augenheilkd; 1971 Dec; 159(6):725-36. PubMed ID: 5159612
    [No Abstract]   [Full Text] [Related]  

  • 18. [The frequency of dento-maxillary anomalies in a group of pre-school children in Timişoara].
    Ghibu-Petcu C
    Stomatologia (Bucur); 1970; 17(4):371-4. PubMed ID: 5271775
    [No Abstract]   [Full Text] [Related]  

  • 19. A genetic study of three rare retinal disorders: dystrophia retinae dysacusis syndrome, x-chromosomal retinoschisis and grouped pigments of the retina.
    Forsius H; Eriksson A; Nuutila A; Vainio-Mattila B; Krause U
    Birth Defects Orig Artic Ser; 1971 Mar; 7(3):83-98. PubMed ID: 5173151
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Primary congenital glaucoma and heredity].
    Daghfous MT; Ayed S; Ben Nejma L; Kamoun S; Boussen S
    Tunis Med; 1986 Oct; 64(10):831-5. PubMed ID: 3824540
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.