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 *

183 related articles for article (PubMed ID: 19161154)

  • 1. Molecular cytogenetic characterization of a 4p15.1-pter duplication and a 4q35.1-qter deletion in a recombinant of chromosome 4 pericentric inversion.
    Maurin ML; Labrune P; Brisset S; Le Lorc'h M; Pineau D; Castel C; Romana S; Tachdjian G
    Am J Med Genet A; 2009 Feb; 149A(2):226-31. PubMed ID: 19161154
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular cytogenetic characterization of the first reported case of an inv dup (4p)(p15.1-pter) with a concomitant 4q35.1-qter deletion and normal parents.
    Tassano E; Alpigiani MG; Salvati P; Gimelli S; Lorini R; Gimelli G
    Gene; 2012 Dec; 511(2):338-40. PubMed ID: 23031810
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins: a genotype-phenotype analysis.
    Ronzoni L; Peron A; Bianchi V; Baccarin M; Guerneri S; Silipigni R; Lalatta F; Bedeschi MF
    Am J Med Genet A; 2015 Jul; 167(7):1551-9. PubMed ID: 25851921
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature review.
    Hemmat M; Hemmat O; Anguiano A; Boyar FZ; El Naggar M; Wang JC; Wang BT; Sahoo T; Owen R; Haddadin M
    Mol Cytogenet; 2013 May; 6(1):17. PubMed ID: 23639048
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Lee MS; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):705-711. PubMed ID: 27751420
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement.
    Preiksaitiene E; Benušienė E; Ciuladaite Z; Šliužas V; Mikštienė V; Kučinskas V
    Taiwan J Obstet Gynecol; 2016 Jun; 55(3):410-4. PubMed ID: 27343325
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Duplication 19q13-qter and deletion 19p13-pter arising from an inversion (19)(p13.3q13.3) of maternal origin.
    López-Exposito I; Guillén-Navarro E; Bafallíu JA; Bernabé MC; Escalona A; Fuster C
    Eur J Med Genet; 2006; 49(6):511-5. PubMed ID: 16824814
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pericentric inversion of chromosome 4 giving rise to dup(4p) and dup(4q) recombinants within a single kindred.
    Hirsch B; Baldinger S
    Am J Med Genet; 1993 Jan; 45(1):5-8. PubMed ID: 8418660
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Recombinant chromosome 4 with partial 4p deletion and 4q duplication inherited from paternal pericentric inversion].
    Mun SJ; Cho EH; Chey MJ; Shim GH; Shin BM; Lee RK; Ko JK; Yoo SJ
    Korean J Lab Med; 2010 Feb; 30(1):89-92. PubMed ID: 20197729
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pre- and postnatal findings in a patient with a recombinant chromosome rec(8)(qter→q21.11::p23.3→qter) due to a paternal pericentric inversion inv(8)(p23.3q21.11) and review of the literature.
    Habhab W; Mau-Holzmann U; Singer S; Rieß A; Kagan KO; Gerbig I; Schäferhoff K; Dufke A; Kehrer M
    Am J Med Genet A; 2020 Nov; 182(11):2680-2684. PubMed ID: 32803851
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4.
    Battaglia A; Brothman AR; Carey JC
    Am J Med Genet; 2002 Sep; 112(1):103-6. PubMed ID: 12239731
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
    Piovani G; Borsani G; Bertini V; Kalscheuer VM; Viertel P; Bellotti D; Valseriati D; Barlati S
    Eur J Med Genet; 2006; 49(3):215-23. PubMed ID: 16762823
    [TBL] [Abstract][Full Text] [Related]  

  • 13. dup(8p)/del(8q) recombinant chromosome in a girl with hepatic focal nodular hyperplasia.
    Tokutomi T; Hayashi S; Imai K; Chida A; Ishiwata T; Asano Y; Inazawa J; Nonoyama S
    Am J Med Genet A; 2007 Jun; 143A(12):1334-7. PubMed ID: 17506094
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A second case of inv(4)pat with both recombinants in the offspring: rec dup(4q) in a girl with Wolf-Hirschhorn syndrome and rec dup(4p).
    Dufke A; Eggermann K; Balg S; Stengel-Rutkowski S; Enders H; Kaiser P
    Cytogenet Cell Genet; 2000; 91(1-4):85-9. PubMed ID: 11173836
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Report of trisomy 2q34-qter and monosomy 4q35.2-qter in a child with mild dysmorphic syndrome and karyotype 46,XY,der(4)t(2;4)(q34;q35.2)pat.
    Meza-Espinoza JP; Sáinz González E; León-León CJN; Arámbula-Meraz E; Contreras-Gutiérrez JA; García-Magallanes N; Madueña-Molina J; Luque-Ortega F; Cervín-Serrano S; Picos-Cárdenas VJ
    Mol Cytogenet; 2020; 13():17. PubMed ID: 32467733
    [TBL] [Abstract][Full Text] [Related]  

  • 16. SALL4 and NFATC2: two major actors of interstitial 20q13.2 duplication.
    Briand-Suleau A; Martinovic J; Tosca L; Tou B; Brisset S; Bouligand J; Delattre V; Giurgea I; Bachir J; Folliot P; Goumy C; Francannet C; Guiochon-Mantel A; Benachi A; Vermeesch J; Tachdjian G; Vago P; Goossens M; Métay C
    Eur J Med Genet; 2014 Mar; 57(4):174-80. PubMed ID: 24486774
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomalies.
    Thienpont B; Gewillig M; Fryns JP; Devriendt K; Vermeesch J
    Cytogenet Genome Res; 2006; 114(3-4):338-41. PubMed ID: 16954676
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Duplication of 20qter and deletion of 20pter due to paternal pericentric inversion: patient report and review of 20qter duplications.
    Starr LJ; Truemper EJ; Pickering DL; Sanger WG; Olney AH
    Am J Med Genet A; 2014 Aug; 164A(8):2020-4. PubMed ID: 24954807
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Recurrent inverted duplication of 2p with terminal deletion in a patient with the classical phenotype of trisomy 2p23-pter.
    Gruchy N; Jacquemont ML; Lyonnet S; Labrune P; El Kamel I; Siffroi JP; Portnoï MF
    Am J Med Genet A; 2007 Oct; 143A(20):2417-22. PubMed ID: 17853488
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
    Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.