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 *

212 related articles for article (PubMed ID: 17330228)

  • 1. Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosis.
    Stumm M; Klopocki E; Gasiorek-Wiens A; Knoll U; Wirjadi D; Sarioglu N; Wegner RD; Tönnies H
    Prenat Diagn; 2007 May; 27(5):475-8. PubMed ID: 17330228
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
    Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 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 and molecular cytogenetic characterisation of a small de novo interstitial duplication 16q11.2-q13.
    Trimborn M; Wegner RD; Tönnies H; Sarioglu N; Albig M; Neitzel H
    Prenat Diagn; 2006 Mar; 26(3):273-6. PubMed ID: 16506262
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis and molecular characterization of an interstitial 1q24.3-31.3 deletion: case report and review.
    Prontera P; Clerici G; Bernardini L; Schippa M; Capalbo A; Manes I; Giuffrida MG; Barbieri MG; Ardisia C; Donti E
    Genet Couns; 2011; 22(1):41-8. PubMed ID: 21614987
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs.
    Giardino D; Corti C; Ballarati L; Finelli P; Valtorta C; Botta G; Giudici M; Grosso E; Larizza L
    Prenat Diagn; 2006 Jun; 26(6):565-70. PubMed ID: 16683274
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Fetoplacental discrepancy involving structural abnormalities of chromosome 8 detected by prenatal diagnosis.
    Soler A; Sánchez A; Carrió A; Badenas C; Milà M; Borrell A
    Prenat Diagn; 2003 Apr; 23(4):319-22. PubMed ID: 12673638
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular characterisation of a prenatally diagnosed 5q15q21.3 deletion and review of the literature.
    Malan V; Martinovic J; Sanlaville D; Caillat S; Waill MC; Ganne ML; Tantau J; Attie-Bitach T; Vekemans M; Morichon-Delvallez N
    Prenat Diagn; 2006 Mar; 26(3):231-8. PubMed ID: 16450350
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis and molecular characterization of an interstitial 1q24.2q25.2 deletion.
    Chaabouni M; Martinovic J; Sanlaville D; Attié-Bittach T; Caillat S; Turleau C; Vekemans M; Morichon N
    Eur J Med Genet; 2006; 49(6):487-93. PubMed ID: 17142120
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: cytogenetic and molecular analysis.
    Velissariou V; Antoniadi T; Patsalis P; Christopoulou S; Hatzipouliou A; Donoghue J; Bakou K; Kaminopetros P; Athanassiou V; Petersen MB
    Prenat Diagn; 2001 Jun; 21(6):484-7. PubMed ID: 11438955
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Complex de novo cryptic subtelomeric rearrangements in a fetus with multiple ultrasonographic abnormalities and a normal karyotype at amniocentesis.
    Iqbal MA; Ramadan S; Ali FA; Kurdi W
    Prenat Diagn; 2005 Dec; 25(12):1142-9. PubMed ID: 16240463
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
    Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
    Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Partial trisomy/monosomy 6q in fetal cells and CVS long-term culture not present in CVS short-term culture.
    Wegner RD; Schröck E; Obladen M; Becker R; Stumm M; Sperling K
    Prenat Diagn; 1996 Aug; 16(8):741-8. PubMed ID: 8878285
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Tetrasomy 12p--unusual presentation in CVS.
    Dong L; Falk RE; Williams J; Kohan M; Schreck RR
    Prenat Diagn; 2003 Feb; 23(2):101-3. PubMed ID: 12575013
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion.
    Prontera P; Aiello V; Toschi M; Turci A; Gruppioni R; Buldrini B; Zago S; Bonfatti A; Donti E; Calzolari E; Sensi A
    Genet Couns; 2007; 18(3):309-15. PubMed ID: 18019372
    [TBL] [Abstract][Full Text] [Related]  

  • 18. First-trimester prenatal diagnosis of a familial subtelomeric translocation.
    Kilby MD; Brackley KJ; Walters JJ; Morton J; Roberts E; Davison EV
    Ultrasound Obstet Gynecol; 2001 Jun; 17(6):531-3. PubMed ID: 11422979
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic hernia.
    Hatem E; Meriam BR; Walid D; Adenen M; Moez G; Ali S
    Prenat Diagn; 2007 May; 27(5):471-4. PubMed ID: 17380471
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping.
    Peschka B; Leygraaf J; Hansmann D; Hansmann M; Schröck E; Ried T; Engels H; Schwanitz G; Schubert R
    Prenat Diagn; 1999 Dec; 19(12):1143-9. PubMed ID: 10590433
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.