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 *

65 related articles for article (PubMed ID: 4008222)

  • 21. Cytogenetic and immunologic abnormalities related to leukemia.
    Hirschhorn K
    Proc Natl Cancer Conf; 1970; 6():107-12. PubMed ID: 5460544
    [No Abstract]   [Full Text] [Related]  

  • 22. [Congenital chromosomal anomalies in 2 children with acute lymphoblastic leukemia].
    Werner-Favre C; Cabrol C; Wyss M; Engel E
    J Genet Hum; 1983 Mar; 31(1):49-51. PubMed ID: 6578297
    [No Abstract]   [Full Text] [Related]  

  • 23. [A case of multiple congenital anomalies with familial C-G translocation].
    Yanagisawa S; Adachi K
    Jinrui Idengaku Zasshi; 1970 Mar; 14(4):309-15. PubMed ID: 5464693
    [No Abstract]   [Full Text] [Related]  

  • 24. [Identification of 2 familial translocations].
    Laurent C; Biemont MC; Robert JM; Dutrillaux B
    Ann Genet; 1974 Dec; 17(4):279-81. PubMed ID: 4548825
    [No Abstract]   [Full Text] [Related]  

  • 25. Chromosomal abnormalities in a patient with adolescent myelofibrosis.
    Moake JL; Lebos H; Warren RJ
    Acta Haematol; 1974; 52(3):173-9. PubMed ID: 4214108
    [No Abstract]   [Full Text] [Related]  

  • 26. [Clinical and chromosomal studies in a congenital hypothyroidism caused by thyroxin synthesis disorders and middle ear hearing disorders (Pendred- or goiter-deafness syndrome)].
    Kitlak W; Gebert P
    Arch Kinderheilkd; 1968; 177(2):170-83. PubMed ID: 5723894
    [No Abstract]   [Full Text] [Related]  

  • 27. A case of a balanced 2/D translocation.
    Lisco E; Lisco H
    Ann Genet; 1967 Mar; 10(1):42. PubMed ID: 5300126
    [No Abstract]   [Full Text] [Related]  

  • 28. [Ring chromosomes in mosaicism 46, XY, Cr-46, XY].
    Ferrier S; Freund M; Grétillat A
    Arch Genet (Zur); 1973; 46(1):1-14. PubMed ID: 4731928
    [No Abstract]   [Full Text] [Related]  

  • 29. [Clonal evolutions and Ph-1: presentation of two cases].
    de Nava C; de Grouchy J; Thoyer C; Bousser J; Bilski-Pasquier J; Freteaux J
    Ann Genet; 1969 Jun; 12(2):83-93. PubMed ID: 5308387
    [No Abstract]   [Full Text] [Related]  

  • 30. Familial agoitrous cretinism accompanied by musclar hypertrophy.
    Cross HE; Hollander CS; Rimoin DL; McKusick VA
    Pediatrics; 1968 Feb; 41(2):413-20. PubMed ID: 5637792
    [No Abstract]   [Full Text] [Related]  

  • 31. Radiation, chromosomes and man.
    Fitzgerald PH
    N Z Med J; 1971 Mar; 73(466):147-54. PubMed ID: 5280738
    [No Abstract]   [Full Text] [Related]  

  • 32. [Syndrome of congenital anomalies in a girl with karyotype 47,XXX].
    Kańska B; Kleczkowska A; Knaus A; Sokolowski J; Stapińska J
    Pediatr Pol; 1971 Jan; 46(1):81-5. PubMed ID: 5545829
    [No Abstract]   [Full Text] [Related]  

  • 33. [Chromosomal changes in ovarian cancer studied by means of differential chromosome staining].
    Chudina AP; Pichugina MN
    Vopr Onkol; 1980; 26(3):88-91. PubMed ID: 6154387
    [No Abstract]   [Full Text] [Related]  

  • 34. [Karyotyping in chronic myeloproliferative syndrome (except chronic myeloid leukemia)].
    Lessard M
    Pathol Biol (Paris); 1982 Nov; 30(9):759-65. PubMed ID: 6760079
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Linkage analysis excludes familial congenital hypothyroidism from chromosome 21.
    Ahlbom BE; Yaqoob M; Annerén G; Larsson A; Ilicki A; Wadelius C
    Genet Couns; 1998; 9(4):265-70. PubMed ID: 9894163
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Cytostatic immunosuppressive therapy, chromosomal aberrations and carcinogenic effect (author's transl)].
    Vormittag W
    Wien Klin Wochenschr; 1974 Feb; 86(3):69-75. PubMed ID: 4439938
    [No Abstract]   [Full Text] [Related]  

  • 37. Unusual chromosomal mosaic (46, XX-46, XX, Cp+) in a girl with multiple malformations.
    Eriksson B; Fraccaro M; Hultén M; Lindsten J; Tiepolo L
    Ann Genet; 1968 Mar; 11(1):6-10. PubMed ID: 5301761
    [No Abstract]   [Full Text] [Related]  

  • 38. [Two observations of identical breakages in the same group C chromosome].
    Emerit I; De Grouchy J; Vernant P
    Ann Genet; 1968 Mar; 11(1):22-7. PubMed ID: 5301752
    [No Abstract]   [Full Text] [Related]  

  • 39. Clinical, cytogeneti and autoradiographic studies in 0 cases with rare chromosome disorders. IV. Cases 9 and 10.
    Moore MK; Engel E
    Ann Genet; 1970 Dec; 13(4):269-74. PubMed ID: 5313392
    [No Abstract]   [Full Text] [Related]  

  • 40. [Familial translocation D/D].
    Colombo A; Forenza N; Maraschio P; Severi F
    Minerva Pediatr; 1975 Oct; 27(31):1706-9. PubMed ID: 1228431
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.