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 *

90 related articles for article (PubMed ID: 22245136)

  • 41. Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpoint.
    De Baere E; Van Roy N; Speleman F; Fukushima Y; De Paepe A; Messiaen L
    Genomics; 1999 Apr; 57(1):70-8. PubMed ID: 10191085
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Breakpoint mapping by FISH in a Sotos patient with a constitutional translocation t(3;6).
    Kok K; Mosselaar A; Faber H; Dijkhuizen T; Draaijers TG; van der Veen AY; Buys CH; Schrander-Stumpel CT
    J Med Genet; 1999 Apr; 36(4):346-7. PubMed ID: 10227409
    [No Abstract]   [Full Text] [Related]  

  • 43. Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome.
    Belloso JM; Bache I; Guitart M; Caballin MR; Halgren C; Kirchhoff M; Ropers HH; Tommerup N; Tümer Z
    Eur J Hum Genet; 2007 Jun; 15(6):711-3. PubMed ID: 17392702
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Id4 is deregulated by a t(6;14)(p22;q32) chromosomal translocation in a B-cell lineage acute lymphoblastic leukemia.
    Bellido M; Aventín A; Lasa A; Estivill C; Carnicer MJ; Pons C; Matías-Guiu X; Bordes R; Baiget M; Sierra J; Nomdedéu JF
    Haematologica; 2003 Sep; 88(9):994-1001. PubMed ID: 12969807
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Two de-novo balanced autosomal translocations after intracytoplasmic sperm injection.
    Lev D; Malinger G; Chaki R; Reichler A; Glazerman M
    Lancet; 1999 Jan; 353(9147):119. PubMed ID: 10023902
    [No Abstract]   [Full Text] [Related]  

  • 46. Tertiary trisomy of 10p15.pter and 14pter.ql3 due to maternal translocation t(10;14)(p15;q13).
    Cetin Z; Mihci E; Keser I; Luleci G
    Genet Couns; 2012; 23(2):207-14. PubMed ID: 22876579
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Isolated Norrie disease in a female caused by a balanced translocation t(X,6).
    Meire FM; Lafaut BA; Speleman F; Hanssens M
    Ophthalmic Genet; 1998 Dec; 19(4):203-7. PubMed ID: 9895245
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Disruption of diacylglycerol kinase delta (DGKD) associated with seizures in humans and mice.
    Leach NT; Sun Y; Michaud S; Zheng Y; Ligon KL; Ligon AH; Sander T; Korf BR; Lu W; Harris DJ; Gusella JF; Maas RL; Quade BJ; Cole AJ; Kelz MB; Morton CC
    Am J Hum Genet; 2007 Apr; 80(4):792-9. PubMed ID: 17357084
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Isolated Robin sequence associated with a balanced t(2;17) chromosomal translocation.
    Jamshidi N; Macciocca I; Dargaville PA; Thomas P; Kilpatrick N; McKinlay Gardner RJ; Farlie PG
    J Med Genet; 2004 Jan; 41(1):e1. PubMed ID: 14729841
    [No Abstract]   [Full Text] [Related]  

  • 50. Disruption of the ATP8A2 gene in a patient with a t(10;13) de novo balanced translocation and a severe neurological phenotype.
    Cacciagli P; Haddad MR; Mignon-Ravix C; El-Waly B; Moncla A; Missirian C; Chabrol B; Villard L
    Eur J Hum Genet; 2010 Dec; 18(12):1360-3. PubMed ID: 20683487
    [TBL] [Abstract][Full Text] [Related]  

  • 51. De novo translocation (1; 2)(q32; p25) associated with bilateral renal dysplasia.
    Joss S; Howatson A; Trainer A; Whiteford M; FitzPatrick DR
    Clin Genet; 2003 Mar; 63(3):239-40. PubMed ID: 12694239
    [No Abstract]   [Full Text] [Related]  

  • 52. Identification of ectodysplasin-A receptor gene deletion at 2q12.2 and a potential autosomal MR locus.
    Griggs BL; Ladd S; Decker A; DuPont BR; Asamoah A; Srivastava AK
    Eur J Hum Genet; 2009 Jan; 17(1):30-6. PubMed ID: 18854857
    [TBL] [Abstract][Full Text] [Related]  

  • 53. De novo 1p35.2 microdeletion including PUM1 identified in a patient with sporadic West syndrome.
    Imaizumi T; Mogami Y; Okamoto N; Yamamoto-Shimojima K; Yamamoto T
    Congenit Anom (Kyoto); 2019 Nov; 59(6):193-194. PubMed ID: 30536491
    [No Abstract]   [Full Text] [Related]  

  • 54. Möbius-like syndrome associated with a 1;2 chromosome translocation.
    Nishikawa M; Ichiyama T; Hayashi T; Furukawa S
    Clin Genet; 1997 Feb; 51(2):122-3. PubMed ID: 9112001
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Rubinstein-taybi syndrome: a female patient with a de novo reciprocal translocation t(2; 16)(q36.3; p13.3) and dysgranulopoiesis.
    Torres LC; de Lourdes Lopes Chauffaille M; Delboni TP; Okay TS; Carneiro-Sampaio M; Sugayama S
    Clinics (Sao Paulo); 2010; 65(1):107-9. PubMed ID: 20126353
    [No Abstract]   [Full Text] [Related]  

  • 56. Amyoplasia associated with a balanced de novo insertion of a segment of the long arm of chromosome 5 into chromosome 2.
    Eisenhut M; Weindling M; Fryer A
    Am J Med Genet; 2002 Feb; 107(4):337-9. PubMed ID: 11840493
    [No Abstract]   [Full Text] [Related]  

  • 57. De novo R853Q mutation of SCN2A gene and West syndrome.
    Samanta D; Ramakrishnaiah R
    Acta Neurol Belg; 2015 Dec; 115(4):773-6. PubMed ID: 25772804
    [No Abstract]   [Full Text] [Related]  

  • 58. Temporal skin folds in a female infant with an unbalanced translocation with breakpoints Xq22.1 and 6p22.3: a new association?
    Vasileiadis GT; Fordham N; Augustynowicz M; Scott RH
    BMJ Case Rep; 2013 Jul; 2013():. PubMed ID: 23833095
    [No Abstract]   [Full Text] [Related]  

  • 59. Disruption of the IQSEC2 transcript in a female with X;autosome translocation t(X;20)(p11.2;q11.2) and a phenotype resembling X-linked infantile spasms (ISSX) syndrome.
    Morleo M; Iaconis D; Chitayat D; Peluso I; Marzella R; Renieri A; Mari F; Franco B
    Mol Med Rep; 2008; 1(1):33-9. PubMed ID: 21479374
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Long non-coding RNAs in cancer.
    Gong Z; Zhang S; Zhang W; Huang H; Li Q; Deng H; Ma J; Zhou M; Xiang J; Wu M; Li X; Xiong W; Li X; Li Y; Zeng Z; Li G
    Sci China Life Sci; 2012 Dec; 55(12):1120-4. PubMed ID: 23233227
    [No Abstract]   [Full Text] [Related]  

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