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 *

94 related articles for article (PubMed ID: 302667)

  • 41. Hereditary spherocytic anemia with deletion of the short arm of chromosome 8.
    Okamoto N; Wada Y; Nakamura Y; Nakayama M; Chiyo H; Murayama K; Inoue T; Kanzaki A; Yawata Y; Hirono A
    Am J Med Genet; 1995 Sep; 58(3):225-9. PubMed ID: 8533822
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin.
    Oner G; Jauch A; Eggermann T; Hardwick R; Kirsch S; Schiebel K; Rappold G; Robson L; Smith A
    Am J Med Genet; 2000 May; 92(2):101-6. PubMed ID: 10797432
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter.
    Cohn AC; Kearns LS; Savarirayan R; Ryan J; Craig JE; Mackey DA
    Ophthalmic Genet; 2005 Mar; 26(1):45-53. PubMed ID: 15823925
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Partial monosomy 22pter leads to q11 in a newborn with the clinical features of trisomy 13 syndrome.
    Back E; Stier R; Böhm N; Adlung A; Hameister H
    Ann Genet; 1980; 23(4):244-8. PubMed ID: 6971606
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Refined mapping of the gene for glutathione reductase on human chromosome 8.
    Gutensohn W; Rodewald A; Haas B; Schulz P; Cleve H
    Hum Genet; 1978 Aug; 43(2):221-4. PubMed ID: 689688
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Partial trisomy for the long arm of chromosome 2 due to malsegregation of a maternal insertion : ins(6;2)(p22;q24q34)].
    Couturier J; Aurias A; Prieur M; Barois A
    Ann Genet; 1977 Mar; 20(1):52-5. PubMed ID: 302675
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Deficiency 10p. Report of a case and exclusion mapping of the hexokinase 1 locus to band 10p11.2.
    Danesino C; Lo Curto F; Bonfant G; Cazzadore C; Voltolin G; Bersi S
    Ann Genet; 1984; 27(3):162-6. PubMed ID: 6334480
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Hereditary 3;6 translocation : three cases of multiple malformations with partial trisomy 6p21 leads to pter.
    Pagano L; Fioretti G; Vetrella M; Risolo E; Casullo C; Celona A; Renda S; Rinaldi A; Ventruto V
    Ann Genet; 1980; 23(3):173-5. PubMed ID: 6968535
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes.
    Crowe CA; Schwartz S; Black CJ; Jaswaney V
    Am J Med Genet; 1997 Sep; 71(4):406-13. PubMed ID: 9286446
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Erythrocyte glutathione reductase activity and acquired trisomy #8 in various hematologic disorders.
    Sadamori N; Takei H; Yao E; Nagamine M; Tomonaga Y; Tagawa M; Kusano M; Ichimaru M
    Cancer Genet Cytogenet; 1984 Jul; 12(3):255-9. PubMed ID: 6722765
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Gene dose effect: regional mapping of human glutathione reductase on chromosome 8.
    George DL; Francke U
    Cytogenet Cell Genet; 1976; 17(5):282-6. PubMed ID: 1017318
    [No Abstract]   [Full Text] [Related]  

  • 52. Increased HK1 activity levels in the red cells of a patient with a de novo trisomy 10p: t(Y;10)(p11;p12).
    Dallapiccola B; Chessa L; Vignetti P; Ferrante E; Gandini E
    Hum Genet; 1979; 50(1):45-9. PubMed ID: 468260
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Exclusion of glutathione reductase from 8pter leads to 8p22 and localization to 8p21.
    Magenis RE; Reiss J; Bigley R; Chamberlin J; Lovrien E
    Cytogenet Cell Genet; 1978; 22(1-6):446-8. PubMed ID: 752521
    [No Abstract]   [Full Text] [Related]  

  • 54. Regional assignment of red cell acid phosphatase locus to band 2p25.
    Junien C; Kaplan JC; Bernheim A; Berger R
    Hum Genet; 1979 Apr; 48(1):17-21. PubMed ID: 457131
    [TBL] [Abstract][Full Text] [Related]  

  • 55. The 8p- syndrome.
    Reiss JA; Brenes PM; Chamberlin J; Magenis RE; Lovrien EW
    Hum Genet; 1979 Mar; 47(2):135-40. PubMed ID: 437781
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Assignment of human uroporphyrinogen I synthase locus to region 11qter by gene dosage effect.
    de Verneuil H; Phung N; Nordmann Y; Allard D; Leprince F; Jérome H; Aurias A; Rethoré MO
    Hum Genet; 1982; 60(3):212-3. PubMed ID: 6985467
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Expression of GALT in 9p chromosome alterations: assignment of GALT locus to 9cen leads to 9p22.
    Sparkes RS; Sparkes MC; Funderburk SJ; Moedjono S
    Ann Hum Genet; 1980 May; 43(4):343-7. PubMed ID: 6249180
    [TBL] [Abstract][Full Text] [Related]  

  • 58. 10q(q23 leads to qter) duplication: GOTs, HK1, and other gene markers.
    Sparkes RS; Bass HN; Sparkes MC
    Hum Genet; 1978 Jun; 42(3):267-70. PubMed ID: 669709
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Clinical, chromosomal and enzymatic studies in four cases of rearrangements of chromosome 7.
    Baeteman MA; Philip N; Mattei MG; Mattei JF
    Clin Genet; 1985 Jun; 27(6):564-9. PubMed ID: 3839444
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Regional mapping of hexokinase-1 within the short arm of chromosome 10.
    Dallapiccola B; Novelli G; Micara G; Delaroche I; Moric-Petrovic S; Magnani M
    Hum Hered; 1984; 34(3):156-60. PubMed ID: 6590458
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.