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 *

123 related articles for article (PubMed ID: 10519353)

  • 41. Evidence for involvement of a Robertsonian translocation 13 chromosome in formation of a ring chromosome 13.
    Stetten G; Tuck-Muller CM; Blakemore KJ; Wong C; Kazazian HH; Antonarakis SE
    Mol Biol Med; 1990 Dec; 7(6):479-84. PubMed ID: 2077349
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Tissue-specific mosaicism for the stability of a ring 13 chromosome.
    McCorquodale MM; Kolacki P; Kurczynski TW; Baugh E
    J Ment Defic Res; 1986 Dec; 30 ( Pt 4)():389-99. PubMed ID: 3806666
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [A report of 2 cases of Turner's syndrome with a ring X chromosome].
    Migliori MV; Bartolotta E; Maurizi M; Bonazzi P; Cardinale G; Manunza V
    Minerva Pediatr; 1991 Sep; 43(9):605-9. PubMed ID: 1758399
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Translocation (16;17)(q22;p13) is a recurrent anomaly of aneurysmal bone cysts.
    Herens C; Thiry A; Dresse MF; Born J; Flagothier C; Vanstraelen G; Allington N; Bex V
    Cancer Genet Cytogenet; 2001 May; 127(1):83-4. PubMed ID: 11408073
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [A case with mosaicism of partial monosomy G- monosomy G in peripheral blood lymphocytes].
    Bauchinger M; Schmid E; Röttinger E
    Humangenetik; 1968; 6(4):303-10. PubMed ID: 5713616
    [No Abstract]   [Full Text] [Related]  

  • 46. [Smith-Magenis syndrome: a case report].
    Quijano Roy S; Delicado Navarro A; López Pajares I; Pascual-Castroviejo I
    An Esp Pediatr; 1998 Oct; 49(4):405-8. PubMed ID: 9859558
    [No Abstract]   [Full Text] [Related]  

  • 47. A case of ring chromosome 15 accompanied by almost normal intelligence.
    Kitatani M; Takahashi H; Ozaki M; Okino E; Maruoka T
    Hum Genet; 1990 Jun; 85(1):138-9. PubMed ID: 2358298
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Triple structural mosaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation.
    Bocian E; Mazurczak T; Buława E; Stańczak H; Rowicka G
    J Med Genet; 1993 Jul; 30(7):614-5. PubMed ID: 8411041
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Partial monosomy 8p and partial trisomy 8p with moderate mental retardation.
    van Balkom ID; Hagendoorn J; De Pater JM; Hennekam RC
    Genet Couns; 1992; 3(2):83-9. PubMed ID: 1642815
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Ring chromosome 22: r(22)].
    Teyssier M; Moreau N
    Bull Assoc Anat (Nancy); 1982 Jun; 66(193):273-82. PubMed ID: 7150788
    [No Abstract]   [Full Text] [Related]  

  • 51. Supernumerary small ring chromosome.
    Lungarotti MS; Calabro A
    J Med Genet; 1978 Dec; 15(6):488. PubMed ID: 745223
    [No Abstract]   [Full Text] [Related]  

  • 52. De novo partial monosomy 21 with unusual karyotype.
    Al-Awadi SA; Naguib KK; Teebi AS; Sundareshan TS
    Jinrui Idengaku Zasshi; 1986 Mar; 31(1):45-8. PubMed ID: 3735757
    [No Abstract]   [Full Text] [Related]  

  • 53. Familial ring (20) chromosomal mosaicism.
    Back E; Voiculescu I; Brünger M; Wolff G
    Hum Genet; 1989 Sep; 83(2):148-54. PubMed ID: 2777254
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Transmission of a ring chromosome 18 from a mother with 46,XX/47,XX, + r(18) mosaicism to her daughter, resulting in a 46,XX,r(18) karyotype.
    Jenderny J; Caliebe A; Beyer C; Grote W
    J Med Genet; 1993 Nov; 30(11):964-5. PubMed ID: 8301656
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Ring chromosome 21. Observation in a female infant.
    Carlo Stella N; Barberi I; Corrado F; Triolo O
    Ann Genet; 1984; 27(4):249-51. PubMed ID: 6335374
    [TBL] [Abstract][Full Text] [Related]  

  • 56. A girl with neurofibromatosis type 1, atypical autism and mosaic ring chromosome 17.
    Havlovicova M; Novotna D; Kocarek E; Novotna K; Bendova S; Petrak B; Hrdlicka M; Sedlacek Z
    Am J Med Genet A; 2007 Jan; 143A(1):76-81. PubMed ID: 17163520
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Cytogenetic analysis and phenotype location analysis on the karyotype of a ring chromosome 21 syndrome].
    Zhu XY; Zhao R; Ye ZC; Peng YG; Tan YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):682-3. PubMed ID: 16331572
    [TBL] [Abstract][Full Text] [Related]  

  • 58. A non-sex chromosome marker in a patient with an atypical Ullrich-Turner phenotype and mosaicism of 46,X,mar/46,XX.
    Gray BA; Bent-Williams A; Wolff DJ; Zori RT
    Clin Genet; 2001 Jul; 60(1):73-6. PubMed ID: 11531974
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Ring chromosome 4.
    McDermott A; Voyce MA; Romain D
    J Med Genet; 1977 Jun; 14(3):228-32. PubMed ID: 881718
    [TBL] [Abstract][Full Text] [Related]  

  • 60. The ring nature of a tiny supernumerary chromosome fragment.
    Hoo JJ; Drummond M; Parslow MI; Chambers D
    Am J Med Genet; 1980; 5(4):331-7. PubMed ID: 7395914
    [TBL] [Abstract][Full Text] [Related]  

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