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 *

125 related articles for article (PubMed ID: 22311498)

  • 1. [Genetic analysis of a supernumerary derivative chromosome 15].
    Wang F; Yang Y; Wang CZ; He XI
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Feb; 29(1):77-81. PubMed ID: 22311498
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
    Tan YQ; Di YF; Song YZ; Cheng DH; Li LY; Lu GX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):392-6. PubMed ID: 17680527
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Analysis of small supernumerary marker chromosome 15q11 in four infertile males].
    Tu XD; Cong XW; Zeng J; Zheng DZ; Yan AZ; Lin YH; Qiu LP; Zhang M; Zhong F; Lan F
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Oct; 30(5):539-43. PubMed ID: 24078566
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Phenotypic and genetic analysis of an inv dup(15) case with a BP3:BP3 rearrangement].
    Zhong F; Lan F; Zhang X; Lin Y; Lin Y; Yan A; Tu X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun; 34(3):402-405. PubMed ID: 28604965
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Array-based comparative genomic hybridization detection of copy number variations in a fetus with hypoplastic left-heart syndrome].
    Wang Y; Ma DY; Yang YQ; Zhou J; Zhou XY; Ji XQ; Chen J; Cao L; Hu P; Xu ZF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):439-42. PubMed ID: 22875502
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification and molecular cytogenetic characterization of a novel complex Y chromosome rearrangement in a boy with disorder of sexual development.
    Dutta UR; Pidugu VK; Goud ChV; Hoefers C; Hagemann M; Dalal A
    Gene; 2013 May; 519(2):374-80. PubMed ID: 23428792
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient.
    Ballarati L; Recalcati MP; Bedeschi MF; Lalatta F; Valtorta C; Bellini M; Finelli P; Larizza L; Giardino D
    Eur J Med Genet; 2009; 52(4):218-23. PubMed ID: 19236961
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Cytogenetic and molecular characterization of partial trisomy 4q and partial monosomy 10q in a patient].
    Zhang YL; Dai Y; Tu ZG; Li QY; Wang LQ; Zhang L; Zeng J; Ouyang ZB
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):153-7. PubMed ID: 20376795
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Cytogenetic analysis and phenotype location analysis on the karyotype of a ring chromosome 21 syndrome].
    Zhu XY; Zhao R; Ye ZC; Peng YG; Tan YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):682-3. PubMed ID: 16331572
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel combined 15q11.2 duplication and a bisatellited supernumerary marker derived from chromosome 22: molecular characterization of the marker.
    Dutta UR; Vempally S; Ranganath P; Dalal A
    Gene; 2014 Apr; 539(1):162-7. PubMed ID: 24508374
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
    Koochek M; Harvard C; Hildebrand MJ; Van Allen M; Wingert H; Mickelson E; Holden JJ; Rajcan-Separovic E; Lewis ME
    Clin Genet; 2006 Feb; 69(2):124-34. PubMed ID: 16433693
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. High resolution microarray CGH and MLPA analysis for improved genotype/phenotype evaluation of two childhood genetic disorder cases: ring chromosome 19 and partial duplication 2q.
    Hermsen MA; Tijssen M; Acero IH; Meijer GA; Ylstra B; Toral JF
    Eur J Med Genet; 2005; 48(3):310-8. PubMed ID: 16179226
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Characterization of an analphoid supernumerary marker chromosome derived from 15q25-->qter using high-resolution CGH and multiplex FISH analyses.
    Huang XL; de Michelena MI; Mark H; Harston R; Benke PJ; Price SJ; Milunsky A
    Clin Genet; 2005 Dec; 68(6):513-9. PubMed ID: 16283881
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).
    Schoumans J; Ruivenkamp C; Holmberg E; Kyllerman M; Anderlid BM; Nordenskjöld M
    J Med Genet; 2005 Sep; 42(9):699-705. PubMed ID: 16141005
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Phenotypic and genetic analysis of a child featuring multiple malformations due to copy number variation on chromosome 5].
    Xue H; Sun X; Lu H; Zhou Y; Guo Y; Zhu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):56-9. PubMed ID: 24510564
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Cytogenetic analysis of a complex chromosomal imbalance 14q+ in a fetus featuring multiple congenital defects].
    Li L; Zhou XY; Ji XQ; Yang YQ; Cao L; Zhou J; Liu A; Cheng J; Liu Y; Hu P; Xu ZF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Apr; 29(2):214-7. PubMed ID: 22487837
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.
    Wyandt HE; Shim SH; Mark HF; Huang XL; Milunsky JM
    Exp Mol Pathol; 2006 Jun; 80(3):262-6. PubMed ID: 16516886
    [TBL] [Abstract][Full Text] [Related]  

  • 19. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays.
    Pinkel D; Segraves R; Sudar D; Clark S; Poole I; Kowbel D; Collins C; Kuo WL; Chen C; Zhai Y; Dairkee SH; Ljung BM; Gray JW; Albertson DG
    Nat Genet; 1998 Oct; 20(2):207-11. PubMed ID: 9771718
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Detection of cryptic subtelomeric chromosome abnormalities and identification of anonymous chromatin using a quantitative multiplex ligation-dependent probe amplification (MLPA) assay.
    Northrop EL; Ren H; Bruno DL; McGhie JD; Coffa J; Schouten J; Choo KH; Slater HR
    Hum Mutat; 2005 Nov; 26(5):477-86. PubMed ID: 16170807
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.