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 *

151 related articles for article (PubMed ID: 7262865)

  • 1. Centromeric instability of chromosomes 1, 9, and 16 associated with combined immunodeficiency.
    Fryns JP; Azou M; Jaeken J; Eggermont E; Pedersen JC; Van den Berghe H
    Hum Genet; 1981; 57(1):108-10. PubMed ID: 7262865
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency.
    Tiepolo L; Maraschio P; Gimelli G; Cuoco C; Gargani GF; Romano C
    Hum Genet; 1979 Oct; 51(2):127-37. PubMed ID: 511139
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Centromeric instability of chromosomes 1 and 16 with variable immune deficiency: a new syndrome.
    Howard PJ; Lewis IJ; Harris F; Walker S
    Clin Genet; 1985 May; 27(5):501-5. PubMed ID: 4006276
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [ICF syndrome. Immunodeficiency, chromosomal centromere instability, facial anomalies. Case report and literature review].
    Kieback P; Wendisch H; Lorenz P; Hinkel K
    Monatsschr Kinderheilkd; 1992 Feb; 140(2):91-4. PubMed ID: 1557060
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Centromeric instability of chromosomes 1, 9 and 16 with variable immune deficiency. Support of a new syndrome.
    Valkova G; Ghenev E; Tzancheva M
    Clin Genet; 1987 Mar; 31(3):119-24. PubMed ID: 3568436
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies.
    Turleau C; Cabanis MO; Girault D; Ledeist F; Mettey R; Puissant H; Prieur M; de Grouchy J
    Am J Med Genet; 1989 Mar; 32(3):420-4. PubMed ID: 2729362
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Juxta-centromeric fragility of chromosomes 1, 2, 9, 16, and immunodeficiency. Special reference to the fragility of chromosome 2 and its oncogenic potential.
    Shabtai F; Klar D; Kimchi D; Antebi E; Hart J; Halbrecht I
    Anticancer Res; 1984; 4(4-5):235-9. PubMed ID: 6486726
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chromosome studies in 5,049 consecutive newborn children.
    Friedrich U; Nielsen J
    Clin Genet; 1973; 4(4):333-43. PubMed ID: 4747810
    [No Abstract]   [Full Text] [Related]  

  • 9. Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndrome.
    Maraschio P; Zuffardi O; Dalla Fior T; Tiepolo L
    J Med Genet; 1988 Mar; 25(3):173-80. PubMed ID: 3351904
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Centromeric heterochromatin instability of chromosomes 1, 9, and 16 in variable immunodeficiency syndrome--a virus-induced phenomenon?
    Haas OA
    Hum Genet; 1990 Jul; 85(2):244-6. PubMed ID: 2196213
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Microdensitometric identification of the pericentric inversion of chromosome No.2 and of duplication of the short arm of chromosome No.7 in a reexamined case.
    Subrt I; Kozák J; Hníková O
    Hum Hered; 1973 Apr; 23(4):331-7. PubMed ID: 4130027
    [No Abstract]   [Full Text] [Related]  

  • 12. Tetrasomy 18p: a distinctive syndrome.
    Rivera H; Möller M; Hernández A; Enríquez-Guerra MA; Arreola R; Cantú JM
    Ann Genet; 1984; 27(3):187-9. PubMed ID: 6334486
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A chromosomal break and partial deletion of a number 9 chromosome.
    Smith GF; Sachdeva S; Justice P
    Hum Hered; 1973; 23(6):561-7. PubMed ID: 4792221
    [No Abstract]   [Full Text] [Related]  

  • 14. Autosomal syndromes.
    Summitt RL
    Pediatr Ann; 1978 Jun; 7(6):94-5, 97-100, 102-7 passim. PubMed ID: 149945
    [No Abstract]   [Full Text] [Related]  

  • 15. A chromosomal breakage syndrome with profound immunodeficiency.
    Conley ME; Spinner NB; Emanuel BS; Nowell PC; Nichols WW
    Blood; 1986 May; 67(5):1251-6. PubMed ID: 2421804
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autosomal polymorphisms.
    Ferguson-Smith MA
    Birth Defects Orig Artic Ser; 1974; 10(10):19-29. PubMed ID: 4142589
    [No Abstract]   [Full Text] [Related]  

  • 17. Ring (13),t(2;6) associated with familial fragile (16).
    Ventruto V; Rinaldi A; Renda S; Stabile M; Rinaldi MM; Cavaliere ML; Conte N; Aveta V
    J Med Genet; 1984 Jun; 21(3):233. PubMed ID: 6748026
    [No Abstract]   [Full Text] [Related]  

  • 18. Early prenatal diagnosis of the ICF syndrome.
    Björck EJ; Bui TH; Wijmenga C; Grandell U; Nordenskjöld M
    Prenat Diagn; 2000 Oct; 20(10):828-31. PubMed ID: 11038463
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Immunoglobulin abnormality in a girl with a large chromosome 18.
    Yanagisawa S
    J Med Genet; 1972 Sep; 9(3):360-5. PubMed ID: 4116772
    [No Abstract]   [Full Text] [Related]  

  • 20. Centromeric instability of chromosome 1 resulting in multibranched chromosomes, telomeric fusions, and "jumping translocations" of 1q in a human immunodeficiency virus-related non-Hodgkin's lymphoma.
    Sawyer JR; Swanson CM; Koller MA; North PE; Ross SW
    Cancer; 1995 Oct; 76(7):1238-44. PubMed ID: 8630904
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.