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 *

134 related articles for article (PubMed ID: 25863095)

  • 1. [Systematic genetic analysis for a case with duplication 9p].
    Zhang J; Li H; Jiang S; Li H; Zhang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr; 32(2):237-9. PubMed ID: 25863095
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
    Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS
    Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Cytogenetic analysis of partial trisomy 9p resulting from a reciprocal balanced 9/21 translocation].
    Wang XR; Luo RL; Dai XH; Liu JY
    Yi Chuan; 2007 Jul; 29(7):813-6. PubMed ID: 17646146
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [A microdeletion of chromosome 9q34.11 may cause suspected cerebral palsy].
    Li H; Chen Y; Li Q; Liu M; Mao J; Song D; Li H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):725-9. PubMed ID: 25449075
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Improved identification for trisomy 9p and partial trisomy 6q presented in a patient by array-based comparative genomic hybridization].
    Zhang J; Cai J; Yang Y; Wang S; Yao F; Huang C; Li H; Li H; Zhang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Dec; 33(6):829-832. PubMed ID: 27984615
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Genetic study of a fetus with 9p direct duplication deletion syndrome].
    Shi S; Lin S; Lou X; Li W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun; 34(3):419-422. PubMed ID: 28604969
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
    Akbas E; Polat S; Karakas-Celik S; Altintas ZM; Yildirim M; Yilgor E
    Genet Couns; 2011; 22(4):417-23. PubMed ID: 22303803
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Determination of trisomy 9p by molecular cytogenetic technology].
    Ding X; Sanoudou D; Yang F; Chen H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Dec; 16(6):383-5. PubMed ID: 10581350
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism.
    Vásquez-Velásquez AI; García-Castillo HA; González-Mercado MG; Dávalos IP; Raca G; Xu X; Dwyer E; Rivera H
    Cytogenet Genome Res; 2011; 132(4):233-8. PubMed ID: 21063078
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A patient with unusual features and a 69.5 Mb duplication from a de novo extra der (9): a case report.
    Zhou YC; Zhang C; Zhai JS; Li TF; Wu QY; Li WW; Li N; Li XJ; Huang YF; Cui YX; Xia XY
    Mol Med Rep; 2015 Jul; 12(1):155-8. PubMed ID: 25760145
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Array-CGH study of partial trisomy 9p without mental retardation.
    Bouhjar IB; Hannachi H; Zerelli SM; Labalme A; Gmidène A; Soyah N; Missaoui S; Sanlaville D; Elghezal H; Saad A
    Am J Med Genet A; 2011 Jul; 155A(7):1735-9. PubMed ID: 21626676
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Genetic diagnosis and analysis of related genes for a pedigree with 2p25 and 12p13 cryptic rearrangements].
    Tu X; Zeng J; Cong X; Yan A; Lin Y; Zhang X; Qiu L; Zhou Y; Lan F
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Aug; 31(4):444-8. PubMed ID: 25119907
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cytogenomic characterization of an unexpected 17.6 Mb 9p deletion associated to a 14.8 Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotype.
    Meloni Vde F; Piazzon FB; Soares Mde F; Takeno SS; Christofolini DM; Kulikowski LD; Brunoni D; Melaragno MI
    Gene; 2012 Mar; 496(1):59-62. PubMed ID: 22285927
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Genetic analysis of a family with super-male syndrome].
    Zhang J; Li H; Jiang S; Chen Y; Zhang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Apr; 31(2):210-3. PubMed ID: 24711034
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.