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 *

132 related articles for article (PubMed ID: 10882757)

  • 1. Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review.
    Heller A; Seidel J; Hübler A; Starke H; Beensen V; Senger G; Rocchi M; Wirth J; Chudoba I; Claussen U; Liehr T
    J Med Genet; 2000 Jul; 37(7):529-32. PubMed ID: 10882757
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Patient with partial trisomy 9q and learning disability but no pyloric stenosis.
    Hengstschläger M; Prusa AR; Repa C; Drahonsky R; Deutinger J; Pollak A; Bernaschek G
    Dev Med Child Neurol; 2004 Jan; 46(1):57-9. PubMed ID: 14974649
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Partial trisomy 9q syndrome with a de novo tandem duplication of 9q22.2-q31.1.
    Utine GE; Melotte C; Vermeesch JR; Fryns JP
    Genet Couns; 2005; 16(4):407-12. PubMed ID: 16440884
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature.
    Sifakis S; Eleftheriades M; Kappou D; Murru R; Konstantinidou A; Orru S; Ziegler M; Liehr T; Manolakos E; Papoulidis I
    Birth Defects Res A Clin Mol Teratol; 2014 Apr; 100(4):284-93. PubMed ID: 24677675
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3-->q31.3) associated with Gorlin syndrome.
    Chen CP; Lin SP; Wang TH; Chen YJ; Chen M; Wang W
    Prenat Diagn; 2006 Aug; 26(8):725-9. PubMed ID: 16927391
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Double partial trisomy 9q34.1-->qter and 21pter-->q22.11: FISH and clinical findings.
    Mattina T; Pierluigi M; Mazzone D; Scardilli S; Perfumo C; Mollica F
    J Med Genet; 1997 Nov; 34(11):945-8. PubMed ID: 9391894
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
    Chen CP; Chern SR; Lin CC; Wang TH; Li YC; Hsieh LJ; Lee CC; Hua HM; Wang W
    Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
    [TBL] [Abstract][Full Text] [Related]  

  • 12. M-FISH applications in clinical genetics.
    Cetin Z; Berker Karaüzüm S; Yakut S; Mihçi E; Baumer A; Wey E; Taçoy S; Bağci G; Lüleci G
    Genet Couns; 2005; 16(3):257-68. PubMed ID: 16259323
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Brief report. Adult patient presenting an interstitial (9) (q21.32q31.1) direct duplication resulting from the malsegregation of a paternal balanced insertional translocation.
    Deng L; Peng Y; Liu J; Wen J; Xia Y; Liang D; Wu L
    Birth Defects Res A Clin Mol Teratol; 2014 Apr; 100(4):294-9. PubMed ID: 24668944
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Characterization of a Complex Chromosomal Rearrangement Involving a de novo Duplication of 9p and 9q and a Deletion of 9q.
    Martín-De Saro MD; Valdés-Miranda JM; Plaza-Benhumea L; Pérez-Cabrera A; Gonzalez-Huerta LM; Guevara-Yañez R; Cuevas-Covarrubias SA
    Cytogenet Genome Res; 2015; 147(2-3):124-9. PubMed ID: 26900692
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotypic and molecular characterization of partial trisomy 2q resulting from insertion-duplication in chromosome 18q: a case report and review of literature.
    Ponnala R; Ranganath P; Dutta UR; Pidugu VK; Dalal AB
    Cytogenet Genome Res; 2012; 136(3):229-34. PubMed ID: 22398442
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial 9q22.3 microduplication spanning PTCH1 causes short stature syndrome with mild intellectual disability and dysmorphic features.
    Izumi K; Hahn A; Christ L; Curtis C; Neilson DE
    Am J Med Genet A; 2011 Jun; 155A(6):1384-9. PubMed ID: 21567912
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Partial trisomy 1q41-qter and partial trisomy 9pter-9q21.32 in a newborn infant: an array CGH analysis and review.
    Akalin I; Bozdag S; Spielmann M; Basaran SY; Nanda I; Klopocki E
    Am J Med Genet A; 2014 Feb; 164A(2):490-4. PubMed ID: 24311106
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotype.
    Mach M; Windpassinger C; Wagner K; Kroisel PM; Petek E
    Genet Couns; 2007; 18(1):9-16. PubMed ID: 17515297
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
    El-Ruby M; Hemly NA; Zaki MS
    Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.