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 *

105 related articles for article (PubMed ID: 4828093)

  • 1. [The 18q-syndrome. Deletion of the long arm of chromosome nr. 18].
    Kroyer S; Niebuhr E; Vestermark S
    Ugeskr Laeger; 1974 Apr; 136(15):827. PubMed ID: 4828093
    [No Abstract]   [Full Text] [Related]  

  • 2. [The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].
    Destiné ML; Punnett HH; Thovichit S; DiGeorge AM; Weiss L
    Ann Genet; 1967 Jun; 10(2):65-9. PubMed ID: 5298975
    [No Abstract]   [Full Text] [Related]  

  • 3. A case of 18q- in a t(18q-;6p+) family.
    Jacobsen P; Mikkelsen M; Niebuhr E; de Grouchy J
    Ann Genet; 1971 Mar; 14(1):41-8. PubMed ID: 5314293
    [No Abstract]   [Full Text] [Related]  

  • 4. The syndrome associated with the partial deletion of the long arms of chromosome 18 (18q-).
    Parker CE; Mavalwala J; Koch R; Hatashita A; Derencsenyi A
    Calif Med; 1972 Oct; 117(4):65-71. PubMed ID: 5075725
    [No Abstract]   [Full Text] [Related]  

  • 5. [Two cases of 18q- syndrome with mosaicism (46,XX / 46,XX, 18q-)].
    Lejeune J; Berger R; Réthoré MO; Lafourcade J; Dutrillaux B; Canlorbe P; Labrune B
    Ann Genet; 1967 Mar; 10(1):18-24. PubMed ID: 5300122
    [No Abstract]   [Full Text] [Related]  

  • 6. [Deficiency of the long arm of chromosome no. 18 (46,XX,18q-)].
    Cenani A; Schoeller L; Schubart G
    Arch Kinderheilkd; 1969 Mar; 178(3):266-72. PubMed ID: 5800650
    [No Abstract]   [Full Text] [Related]  

  • 7. [Familial occurrence of long arm deletion in chromosome 18 (46,18q-)].
    Dziuba P; Jończyk K; Dziekanowska D; Bulsiewicz H
    Pediatr Pol; 1972 Aug; 47(8):1037-42. PubMed ID: 5074000
    [No Abstract]   [Full Text] [Related]  

  • 8. Interstitial deletion of the long arm of chromosome 2: case report and review of literature.
    Taysi K; Dengler DR; Jones LA; Heersma JR
    Ann Genet; 1981; 24(4):245-7. PubMed ID: 7036843
    [No Abstract]   [Full Text] [Related]  

  • 9. [18q-syndrome. Karyotype-phenotype correlation in the maxillofacial region].
    Feichtinger C; Rossiwall B
    Osterr Z Stomatol; 1974 Feb; 71(2):42-53. PubMed ID: 4532743
    [No Abstract]   [Full Text] [Related]  

  • 10. [Wolf syndrome. Apropos of 2 cases].
    García González P; Pedraz García C; Merino Marcos L; Salazar Veloz J; Escudero Bueno G; Salazar Villalobos V
    An Esp Pediatr; 1983 Feb; 18(2):113-7. PubMed ID: 6881733
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A case with short arm deletion of chromosome 18 (18p-syndrome).
    Kumagai M; Kikuchi Y; Oishi H; Matsuda E; Kato J
    Jinrui Idengaku Zasshi; 1973 Jun; 18(1):24-36. PubMed ID: 4796358
    [No Abstract]   [Full Text] [Related]  

  • 12. Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature.
    de Die-Smulders CE; Engelen JJ; Schrander-Stumpel CT; Govaerts LC; de Vries B; Vles JS; Wagemans A; Schijns-Fleuren S; Gillessen-Kaesbach G; Fryns JP
    Am J Med Genet; 1995 Nov; 59(3):369-74. PubMed ID: 8599364
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A supposed deletion in the long arm of one of the group B chromosomes in a peculiar form of oligophrenia].
    Grinberg KN; Podugol'nikova OA; Lebedinskaia KS; Bliumina MG; Raĭskaia MM
    Tsitologiia; 1966; 8(2):319-26. PubMed ID: 5984081
    [No Abstract]   [Full Text] [Related]  

  • 14. [Chromosome 18 long arm deletion. A case with unusual dermatoglyphics].
    Le Marec B; Lessard M; Renault A; Coutel Y
    Pediatrie; 1971; 26(7):749-57. PubMed ID: 5118994
    [No Abstract]   [Full Text] [Related]  

  • 15. [A case of 18q-syndrome].
    Lejeune J; Berger R; Rethoré MO; Vialatte J
    J Genet Hum; 1969 Oct; 17(3):423-8. PubMed ID: 5387418
    [No Abstract]   [Full Text] [Related]  

  • 16. [Chromosomal mosaicism in the r (15) syndrome].
    Malygina NA; Mutovin GR; Filina NP; Akif'ev AP
    Genetika; 1980; 16(11):2029-33. PubMed ID: 7193157
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A case of partial deletion of the long arm of chromosome 7 (7q34 leads to 7qter).
    Nistrup Madsen H; Lundsteen C; Steinrud J
    Dan Med Bull; 1983 Feb; 30(1):14-6. PubMed ID: 6831934
    [No Abstract]   [Full Text] [Related]  

  • 18. 18q- and 18q+ mosaicism in a mentally retarded boy.
    Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF
    Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Isochromosome-formation in chromosome 9.
    Miller K; Arslan-Kirchner M
    Ann Genet; 1994; 37(2):78-81. PubMed ID: 7985983
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [18 Q-syndrome. A new case of partial deletion of the long arm of chromosome 18].
    Bourgeois M; Broustet A; Benezech M
    Ann Med Psychol (Paris); 1974 May; 1(5):641-8. PubMed ID: 4433110
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.