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 *

78 related articles for article (PubMed ID: 18615545)

  • 1. Prenatal diagnosis of a de novo partial trisomy 10p12.1-12.2 pter originating from an unbalanced translocation onto 15qter and confirmed with array CGH.
    Kitsiou-Tzeli S; Sismani C; Karkaletsi M; Florentin L; Anastassiou A; Koumbaris G; Evangelidou P; Agapitos E; Patsalis PC; Velissariou V
    Prenat Diagn; 2008 Aug; 28(8):770-2. PubMed ID: 18615545
    [No Abstract]   [Full Text] [Related]  

  • 2. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
    Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
    Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal findings and delineation of de novo concurrent partial trisomy 7q(7q31.2 --> qter) and partial monosomy 6q(6q26 --> qter) by high-resolution array CGH.
    Choy KW; Chan LW; Tang MH; Ng LK; Leung TY; Lau TK
    J Matern Fetal Neonatal Med; 2009 Nov; 22(11):1014-20. PubMed ID: 19900039
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation.
    Simovich MJ; Yatsenko SA; Kang SH; Cheung SW; Dudek ME; Pursley A; Ward PA; Patel A; Lupski JR
    Prenat Diagn; 2007 Dec; 27(12):1112-7. PubMed ID: 17849500
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.
    Machado IN; Heinrich JK; Campanhol C; Rodrigues-Peres RM; Oliveira FM; Barini R
    Genet Mol Res; 2010 Mar; 9(1):441-8. PubMed ID: 20391329
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Partial chromosome deletion: a new trisomy rescue mechanism?
    Vialard F; Molina-Gomes D; Quarello E; Leroy B; Ville Y; Selva J
    Fetal Diagn Ther; 2009; 25(1):111-4. PubMed ID: 19246929
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial trisomy 20p resulting from recombination of a maternal pericentric inversion: case report of a prenatal diagnosis by chorionic villus sampling.
    Molina-Gomes D; Nebout V; Daikha-Dahmane F; Vialard F; Ville Y; Selva J
    Prenat Diagn; 2006 Mar; 26(3):239-41. PubMed ID: 16485319
    [TBL] [Abstract][Full Text] [Related]  

  • 8. First prenatal diagnosis of partial trisomy 10 and partial monosomy 15 derived from a maternal translocation (10;15)(q11;q13).
    Martin-Denavit T; Attia-Sobol J; Theuil J; Abel-Lablanche K; Boggio D; Teyssier M; Till M; Champion F; Vitrey D; Plauchu H
    Prenat Diagn; 2002 Jun; 22(6):487-9. PubMed ID: 12116308
    [No Abstract]   [Full Text] [Related]  

  • 9. Prenatal diagnosis of 47,XX,der(15)t(15;16)(q13;p13.2).
    Santolaya-Forgas J; De Leon J; Powell WC; Tonk V
    Prenat Diagn; 2004 Mar; 24(3):209-12. PubMed ID: 15057955
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Efficacy of array comparative genomic hybridization in a fetus with an inherited apparently balanced translocation: A case report.
    Park JK; Lee JI; Jo HC; Shin JK; Lee SA; Lee JH; Paik WY
    J Obstet Gynaecol Res; 2008 Aug; 34(4 Pt 2):653-7. PubMed ID: 18840174
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 'Pure' partial trisomy 4q26-->q35.2 resulting from a familial unbalanced translocation t(4;10)(q26;q26.3).
    Zhang YL; Dai Y; Tu ZG; Li QY
    Cytogenet Genome Res; 2009; 127(1):67-72. PubMed ID: 20145385
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of monosomy 4p14-->pter and trisomy 11q25-->qter: clinical presentations and outcomes.
    Peng HH; Wang TH; Chao AS; Chang YL; Chang SD; Soong YK
    Prenat Diagn; 2005 Dec; 25(12):1133-7. PubMed ID: 16231301
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter).
    Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Chern SR; Lee CC; Chen YJ; Wang W
    Prenat Diagn; 2005 Dec; 25(12):1170-2. PubMed ID: 16315335
    [No Abstract]   [Full Text] [Related]  

  • 14. Trisomy 2 due to a 3:1 segregation in an abortion studied by QF-PCR and CGH.
    Lorda-Sánchez I; Diego-Alvarez D; Ayuso C; de Alba MR; Trujillo MJ; Ramos C
    Prenat Diagn; 2005 Oct; 25(10):934-8. PubMed ID: 16088866
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.
    Semerci CN; Bahce M; Atik F; Candemir Z; Kiraz IK; Zorlu P; Gül D
    Ann Genet; 2004; 47(4):393-8. PubMed ID: 15581838
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Partial trisomy 13 due to t(X;13) translocation. Contribution of in situ hybridization].
    Bourrouillou G; Mattei MG; Calvas P; Le Tallec JY; Racine A; Rivière M; Rivière C; Carrière JP; Colombies P
    Ann Genet; 1987; 30(3):158-63. PubMed ID: 3499853
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Unbalanced chromosomal translocation: a cause of recurrent spontaneous abortion.
    Zarina AL; Jamil MA; Ng SP; Rohana J; Yong SC; Salwati S; Boo NY
    Med J Malaysia; 2006 Jun; 61(2):260-2. PubMed ID: 16898328
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Characterization of two add(4qter) chromosomes by comparative genomic hybridization.
    Bocéno M; Rival JM; Nomballais MF; David A; Avet-Loiseau H
    Ann Genet; 1998; 41(2):83-6. PubMed ID: 9706338
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Trisomy 12 mosaicism in CVS culture confirmed in the fetus.
    Sikkema-Raddatz B; Bouman K; Verschuuren-Bemelmans CC; de Jong B
    Prenat Diagn; 1999 Dec; 19(12):1176-7. PubMed ID: 10590440
    [No Abstract]   [Full Text] [Related]  

  • 20. A rare case of de novo distal 19q trisomy prenatally diagnosed.
    Rombout S; Sartenaer D; Parmentier B; Dugauquier C; Gillerot Y
    Prenat Diagn; 2004 Oct; 24(10):822-7. PubMed ID: 15503276
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.