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 *

136 related articles for article (PubMed ID: 4181852)

  • 1. The frequency of conditions due to mutant genes of large effect.
    Carter CO
    Lancet; 1969 Jun; 1(7607):1203-6. PubMed ID: 4181852
    [No Abstract]   [Full Text] [Related]  

  • 2. [Regional characteristics of the incidence of hereditary pathology in Uzbekistan].
    Gar'kavtseva RF; Ginter EK; Revazov AA
    Vestn Akad Med Nauk SSSR; 1984; (7):69-75. PubMed ID: 6236633
    [No Abstract]   [Full Text] [Related]  

  • 3. Genetic counseling.
    Wilson MG
    Curr Probl Pediatr; 1975 May; 5(7):1-51. PubMed ID: 1093815
    [No Abstract]   [Full Text] [Related]  

  • 4. Genetic counseling.
    Degnan M; Peters J; Porter IH; Gottesman DM
    Am Fam Physician; 1975 Jul; 12(1):111-7. PubMed ID: 125534
    [No Abstract]   [Full Text] [Related]  

  • 5. Genetic counseling. Considerations for talking to parents and prospective parents.
    Gordon H
    JAMA; 1971 Aug; 217(9):1215-25. PubMed ID: 5109460
    [No Abstract]   [Full Text] [Related]  

  • 6. [Association of chronic tubulo-interstitial nephropathy and of tapeto-retinal degeneration. Genetic study].
    Bois E; Royer P
    Arch Fr Pediatr; 1970 May; 27(5):471-81. PubMed ID: 5425823
    [No Abstract]   [Full Text] [Related]  

  • 7. The evaluation of chemical mutagenicity data in relation to population risk: impact of various types of genetic damage and risk assessment.
    Crow JF
    Environ Health Perspect; 1973 Dec; 6():1-5. PubMed ID: 4780781
    [No Abstract]   [Full Text] [Related]  

  • 8. Fourteen genetic misconceptions.
    McKusick VA
    Ann Intern Med; 1971 Oct; 75(4):642-3. PubMed ID: 5094079
    [No Abstract]   [Full Text] [Related]  

  • 9. The fate of gene mutations and their impact on human sex ratio.
    Larsson T
    Acta Psychiatr Scand; 1973; 49(3):281-93. PubMed ID: 4715073
    [No Abstract]   [Full Text] [Related]  

  • 10. The susceptibility of the fetus and child to chemical pollutants. Monitoring for human mutagenesis.
    Sutton HE
    Pediatrics; 1974 May; 53(5):800-7. PubMed ID: 4416527
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. Genetic disorders.
    Nevin NC
    Clin Obstet Gynaecol; 1982 Apr; 9(1):3-27. PubMed ID: 7049498
    [No Abstract]   [Full Text] [Related]  

  • 13. Genetic counselling.
    Carter CO
    Lancet; 1969 Jun; 1(7609):1303-5. PubMed ID: 4182191
    [No Abstract]   [Full Text] [Related]  

  • 14. Public health and long-term genetic implications of intrauterine diagnosis and selective abortion.
    Motulsky AG; Fraser GR; Felsenstein J
    Birth Defects Orig Artic Ser; 1971 Apr; 7(5):22-32. PubMed ID: 5120222
    [No Abstract]   [Full Text] [Related]  

  • 15. Familial Hyperkalemia and Hypertension (FHHt) and KLHL3: Description of a Family with a New Recessive Mutation (S553L) Compared to a Family with a Dominant Mutation, Q309R, with Analysis of Urinary Sodium Chloride Cotransporter.
    Kliuk-Ben Bassat O; Carmon V; Hanukoglu A; Ganon L; Massalha E; Holtzman EJ; Farfel Z; Mayan H
    Nephron; 2017; 137(1):77-84. PubMed ID: 28511177
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Disease susceptibility genes--their identification by multiple case family studies.
    Day NE; Simons MJ
    Tissue Antigens; 1976 Aug; 8(2):109-19. PubMed ID: 968896
    [No Abstract]   [Full Text] [Related]  

  • 17. From gene to phene.
    Porter IH
    J Invest Dermatol; 1973 Jun; 60(6):360-8. PubMed ID: 4268033
    [No Abstract]   [Full Text] [Related]  

  • 18. Dentinogenesis imperfecta: severe expression in a probable homozygote.
    Shokeir MH
    Clin Genet; 1972; 3(6):442-7. PubMed ID: 4650865
    [No Abstract]   [Full Text] [Related]  

  • 19. Genetic diseases among Jews.
    Adam A
    Isr J Med Sci; 1973; 9(9):1383-92. PubMed ID: 4590458
    [No Abstract]   [Full Text] [Related]  

  • 20. A novel mutation in the calcium sensing receptor gene in a neonate with severe hyperparathyroidism.
    Kahvecioglu D; Atasay B; Berberoglu M; Yildiz D; Cakir U; Akduman H; Erdeve O; Siklar Z; Magdelaine C; Lienhardt-Roussie A; Akar M; Ozbek MN; Arsan S
    Genet Couns; 2014; 25(3):331-5. PubMed ID: 25365856
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.