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 *

158 related articles for article (PubMed ID: 26697114)

  • 1. Copy number changes and methylation patterns in an isodicentric and a ring chromosome of 15q11-q13: report of two cases and review of literature.
    Wang Q; Wu W; Xu Z; Luo F; Zhou Q; Li P; Xie J
    Mol Cytogenet; 2015; 8():97. PubMed ID: 26697114
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chromosome 15q11-q13 copy number gain detected by array-CGH in two cases with a maternal methylation pattern.
    Tan ES; Yong MH; Lim EC; Li ZH; Brett MS; Tan EC
    Mol Cytogenet; 2014; 7():32. PubMed ID: 24959201
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
    Depienne C; Moreno-De-Luca D; Heron D; Bouteiller D; Gennetier A; Delorme R; Chaste P; Siffroi JP; Chantot-Bastaraud S; Benyahia B; Trouillard O; Nygren G; Kopp S; Johansson M; Rastam M; Burglen L; Leguern E; Verloes A; Leboyer M; Brice A; Gillberg C; Betancur C
    Biol Psychiatry; 2009 Aug; 66(4):349-59. PubMed ID: 19278672
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome.
    Chen CP; Ko TM; Chen YY; Su JW; Wang W
    Gene; 2013 Sep; 527(1):384-8. PubMed ID: 23747353
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15.
    Wang NJ; Parokonny AS; Thatcher KN; Driscoll J; Malone BM; Dorrani N; Sigman M; LaSalle JM; Schanen NC
    BMC Genet; 2008 Jan; 9():2. PubMed ID: 18177502
    [TBL] [Abstract][Full Text] [Related]  

  • 6. PWS/AS MS-MLPA Confirms Maternal Origin of 15q11.2 Microduplication.
    Dawson AJ; Cox J; Hovanes K; Spriggs E
    Case Rep Genet; 2015; 2015():474097. PubMed ID: 26064710
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular diagnosis of Prader-Willi and Angelman syndromes by methylation-specific melting analysis and methylation-specific multiplex ligation-dependent probe amplification.
    Procter M; Chou LS; Tang W; Jama M; Mao R
    Clin Chem; 2006 Jul; 52(7):1276-83. PubMed ID: 16690734
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.
    Chen CP; Chen M; Ko TM; Ma GC; Tsai FJ; Tsai MS; Wu PC; Lee CC; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2010 Dec; 49(4):500-5. PubMed ID: 21199754
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
    Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Wu PC; Chen WL; Chen LF; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):188-95. PubMed ID: 21791306
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).
    Christian SL; Fantes JA; Mewborn SK; Huang B; Ledbetter DH
    Hum Mol Genet; 1999 Jun; 8(6):1025-37. PubMed ID: 10332034
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Variation analysis of the number of copies and methylene patterns in region 15q11-q13].
    Laurito S; Roqué M
    Medicina (B Aires); 2018; 78(1):1-5. PubMed ID: 29360068
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities.
    Chen CP; Lin SP; Lin YH; Chern SR; Wu PS; Chen YN; Chen SW; Yang CW; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):852-855. PubMed ID: 28040132
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing.
    Lebedev IN; Karamysheva TV; Elisaphenko EA; Makunin AI; Zhigalina DI; Lopatkina ME; Drozdov GV; Cheremnykh AD; Torkhova NB; Seitova GN; Vasilyev SA; Kashevarova AA; Nazarenko LP; Rubtsov NB
    Biomedicines; 2021 Aug; 9(8):. PubMed ID: 34440234
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. [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]  

  • 16. Complex de novo chromosomal rearrangement at 15q11-q13 involving an intrachromosomal triplication in a patient with a severe neuropsychological phenotype: clinical report and review of the literature.
    Castronovo C; Crippa M; Bestetti I; Rusconi D; Russo S; Larizza L; Sangermani R; Bonati MT; Finelli P
    Am J Med Genet A; 2015 Jan; 167A(1):221-30. PubMed ID: 25339188
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
    Chen CP; Chen M; Chern SR; Wu PS; Chang SP; Lee DJ; Chen YT; Chen LF; Su JW; Hwa-Ruey Hsieh A; Hwa-Jiun Hsieh A; Wang W
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):411-7. PubMed ID: 23040927
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.
    Melo JB; Matoso E; Polityko A; Saraiva J; Backx L; Vermeesch JR; Kosyakova N; Ewers E; Liehr T; Carreira IM
    Cytogenet Genome Res; 2009; 125(2):109-14. PubMed ID: 19729913
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Methylation-specific multiplex ligation-dependent probe amplification in diagnosis of Prader-Willi syndrome and Angelman syndrome].
    Li MR; Wang XZ; Liu XY; Yang YL; Bao XH; Zhang YH; Xiong H; Zhong N; Qin J; Wu XR; Pan H
    Zhonghua Yi Xue Za Zhi; 2008 Dec; 88(46):3257-61. PubMed ID: 19159549
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.