BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

263 related articles for article (PubMed ID: 10190483)

  • 1. De novo inverted duplication 9p21pter involving telomeric repeated sequences.
    Sanlaville D; Baumann C; Lapierre JM; Romana S; Collot N; Cacheux V; Turleau C; Tachdjian G
    Am J Med Genet; 1999 Mar; 83(2):125-31. PubMed ID: 10190483
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular characterisation of a mosaicism with a complex chromosome rearrangement: evidence for coincident chromosome healing by telomere capture and neo-telomere formation.
    Chabchoub E; Rodríguez L; Galán E; Mansilla E; Martínez-Fernandez ML; Martínez-Frías ML; Fryns JP; Vermeesch JR
    J Med Genet; 2007 Apr; 44(4):250-6. PubMed ID: 17172463
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal Diagnosis of Trisomy 2p due to Terminal 2p Duplication including Interstitial Telomeric Sequences.
    Marlet L; Alix E; Till M; Raskin-Champion F; Attia J; Boggio D; Sanlaville D; Schluth-Bolard C
    Cytogenet Genome Res; 2017; 153(3):117-124. PubMed ID: 29268249
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular cytogenetic characterization and origin of two de novo duplication 9p cases.
    Tsezou A; Kitsiou S; Galla A; Petersen MB; Karadima G; Syrrou M; Sahlèn S; Blennow E
    Am J Med Genet; 2000 Mar; 91(2):102-6. PubMed ID: 10748406
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Phenotypic and cytogenetic spectrum of 9p trisomy.
    Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
    Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplication.
    Moog U; Engelen JJ; de Die-Smulders CE; Albrechts JC; Loneus WH; Haagen AA; Raven EJ; Hamers AJ
    Clin Genet; 1994 Dec; 46(6):423-9. PubMed ID: 7889659
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pure 9p trisomy derived from a terminal balanced unreciprocal translocation.
    Brambila-Tapia AJ; Neira VA; Vásquez-Velásquez AI; Jimenez-Arredondo RE; Chávez-González EL; Picos-Cárdenas VJ; Fletes-Rayas AL; Figuera LE
    Genet Couns; 2014; 25(3):289-97. PubMed ID: 25365851
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization.
    Guo WJ; Callif-Daley F; Zapata MC; Miller ME
    Am J Med Genet; 1995 Sep; 58(3):230-6. PubMed ID: 8533823
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).
    Petit P; Devriendt K; Vermeesch JR; Meireleire J; Fryns JP
    Genet Couns; 1998; 9(3):215-21. PubMed ID: 9777345
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Large duplication 4q25-q34 with mild clinical effect.
    Elghezal H; Sendi HS; Monastiri K; Lapierre JM; Romdhane SI; Mougou S; Saad A
    Ann Genet; 2004; 47(4):419-22. PubMed ID: 15581841
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Trisomy of the short arm of chromosome 5 due to a de novo inversion and duplication (5)(p15.3 p13.3).
    Cervera M; Sánchez S; Molina B; Alcántara MA; Del Castillo V; Carnevale A; González-del Angel A
    Am J Med Genet A; 2005 Aug; 136A(4):381-5. PubMed ID: 16001443
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cytogenetic and array-CGH characterization of a complex de novo rearrangement involving duplication and deletion of 9p and clinical findings in a 4-month-old female.
    Hulick PJ; Noonan KM; Kulkarni S; Donovan DJ; Listewnik M; Ihm C; Stoler JM; Weremowicz S
    Cytogenet Genome Res; 2009; 126(3):305-12. PubMed ID: 20068300
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Complex rearrangement involving 9p deletion and duplication in a syndromic patient: genotype/phenotype correlation and review of the literature.
    Recalcati MP; Bellini M; Norsa L; Ballarati L; Caselli R; Russo S; Larizza L; Giardino D
    Gene; 2012 Jul; 502(1):40-5. PubMed ID: 22537675
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Another rare case of a child with de novo terminal 9p deletion and co-existing interstitial 9p duplication: clinical findings and molecular cytogenetic study by array-CGH.
    Kowalczyk M; Tomaszewska A; Podbioł-Palenta A; Constantinou M; Wawrzkiewicz-Witkowska A; Kowalski J; Kałużewski B; Zajączek S; Srebniak MI
    Cytogenet Genome Res; 2013; 139(1):9-16. PubMed ID: 22965227
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotype.
    Erdel M; Duba HC; Verdorfer I; Lingenhel A; Geiger R; Gutenberger KH; Ludescher E; Utermann B; Utermann G
    Hum Genet; 1997 May; 99(5):596-601. PubMed ID: 9150724
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification and characterization of a de novo partial trisomy 10p by comparative genomic hybridization (CGH).
    Benzacken B; Lapierre JM; Siffroi JP; Chalvon A; Tachdjian G
    Clin Genet; 1998 Oct; 54(4):334-40. PubMed ID: 9831346
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inverted duplication deletion of 8P: characterization by standard cytogenetic and SNP array analyses.
    Sireteanu A; Braha E; Popescu R; Gramescu M; Gorduza EV; Rusu C
    Rev Med Chir Soc Med Nat Iasi; 2013; 117(3):731-4. PubMed ID: 24502041
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 --> pter and partial trisomy 1q41 --> qter suggests neo-telomere formation in stabilizing the deleted chromosome.
    Kulikowski LD; Christ LA; Nogueira SI; Brunoni D; Schwartz S; Melaragno MI
    Am J Med Genet A; 2006 Jan; 140(1):82-7. PubMed ID: 16333825
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24).
    Haddad BR; Lin AE; Wyandt H; Milunsky A
    J Med Genet; 1996 Dec; 33(12):1045-7. PubMed ID: 9004142
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Loss of subtelomeric sequence associated with a terminal inversion duplication of the short arm of chromosome 4.
    Cotter PD; Kaffe S; Li L; Gershin IF; Hirschhorn K
    Am J Med Genet; 2001 Jul; 102(1):76-80. PubMed ID: 11471177
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.