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 *

128 related articles for article (PubMed ID: 6570667)

  • 21. The chromosome, its anatomy, and its aberrations.
    Yang-Feng TL
    Res Publ Assoc Res Nerv Ment Dis; 1991; 69():19-38. PubMed ID: 2003160
    [No Abstract]   [Full Text] [Related]  

  • 22. H-Y antigen in human X-autosome translocations.
    Mayerova A; Zuffardi O; Maraschio P; Muller U; Sperling K; Ropers HH; Fraccaro M; Wolf U
    Acta Anthropogenet; 1983; 7(2):119-31. PubMed ID: 6611162
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular biology of neurological diseases.
    Cumming WJ
    Postgrad Med J; 1992 Apr; 68(798):237-41. PubMed ID: 1357639
    [No Abstract]   [Full Text] [Related]  

  • 24. An infant with double trisomy (48,XXX, + 18).
    Jaruratanasirikul S; Jinorose U
    Am J Med Genet; 1994 Jan; 49(2):207-10. PubMed ID: 8116670
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A guide to human chromosome defects.
    Babu A; Hirschhorn K
    Birth Defects Orig Artic Ser; 1992; 28(2):1-18. PubMed ID: 1294260
    [No Abstract]   [Full Text] [Related]  

  • 26. Intriguing association between disease associated unstable trinucleotide repeat and CpG island.
    Gourdon G; Dessen P; Lia AS; Junien C; Hofmann-Radvanyi H
    Ann Genet; 1997; 40(2):73-7. PubMed ID: 9259953
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetics for the cardiologist. Part I: mendelian inheritance.
    Rowley PT
    Mod Concepts Cardiovasc Dis; 1978 Jan; 47(1):63-6. PubMed ID: 634264
    [No Abstract]   [Full Text] [Related]  

  • 28. [Single-factor heredity. Construction and interpretation of a genealogical tree. Principles of genetic counseling].
    Eydoux P
    Rev Prat; 1991 Dec; 41(25):2645-53. PubMed ID: 1803482
    [No Abstract]   [Full Text] [Related]  

  • 29. [Methods and indications for prenatal diagnosis. I. Elements of human genetics].
    Masse A
    Union Med Can; 1983 Aug; 112(8):708-10, 712-3, 721. PubMed ID: 6636360
    [No Abstract]   [Full Text] [Related]  

  • 30. Cancer genetics. II. Studies in humans. Problems in human studies.
    Lynch HT
    Nebr Med J; 1973 Nov; 58(11):401-7. PubMed ID: 4585611
    [No Abstract]   [Full Text] [Related]  

  • 31. Human chromosomes--normal and abnormal.
    Irfan H
    Curr Med Drugs; 1968 Apr; 8(8):3-15. PubMed ID: 5728656
    [No Abstract]   [Full Text] [Related]  

  • 32. The morbid anatomy of the human genome: a review of gene mapping in clinical medicine (3).
    McKusick VA
    Medicine (Baltimore); 1987 Jul; 66(4):237-96. PubMed ID: 3298930
    [No Abstract]   [Full Text] [Related]  

  • 33. [Description of a case of ring chromosome 21 and pericentric inversion of Y chromosome].
    Ponzio G; Carozzi F; Dragone E; Spada A; Brignone S; De Marchi M; Carbonara A
    Pathologica; 1983; 75 Suppl():276-9. PubMed ID: 6680430
    [No Abstract]   [Full Text] [Related]  

  • 34. [An update of molecular genetics in medicine].
    Salamanca Gómez F; Carnevale A; Kofman-Alfaro S; López López M; Torres Maldonado LC; Armendares S; Lisker R
    Gac Med Mex; 1993; 129(4):273-89. PubMed ID: 7926415
    [No Abstract]   [Full Text] [Related]  

  • 35. [Analysis of disease-associated marker chromosomes using chromosome sorter].
    Minoshima S; Shimizu N
    Tanpakushitsu Kakusan Koso; 1996 Nov; 41(15 Suppl):2174-81. PubMed ID: 8952379
    [No Abstract]   [Full Text] [Related]  

  • 36. Pseudogout: session II. Genetics of CPPD deposition: discussion.
    Arthritis Rheum; 1976; 19 Suppl 3():410-1. PubMed ID: 938603
    [No Abstract]   [Full Text] [Related]  

  • 37. [The type of inheritance of anhidrotic ectodermal dysplasia].
    Al'tshuler BA; Suvorova KN
    Vestn Dermatol Venerol; 1984 Feb; (2):15-8. PubMed ID: 6720063
    [No Abstract]   [Full Text] [Related]  

  • 38. [Clinical and genetic aspects of fertility disorders of chromosome origin].
    Goebel KM; Hausmann L; Kaffarnik H
    Minerva Med; 1970 Dec; 61(100):5769-75. PubMed ID: 5531804
    [No Abstract]   [Full Text] [Related]  

  • 39. [Development of cytogenetic methodology: contributions to the knowledge of chromosome structure and its application in clinical practice].
    Salamanca-Gómez F
    Gac Med Mex; 1983 Aug; 119(8):315-25. PubMed ID: 6680106
    [No Abstract]   [Full Text] [Related]  

  • 40. Hereditary vitreoretinal degenerations.
    Neetens A
    Bull Soc Belge Ophtalmol; 1987; 223 Pt 2():9-16. PubMed ID: 3502798
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.