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 *

97 related articles for article (PubMed ID: 31590400)

  • 1. Possible Phenotypic Consequences of Structural Differences in Idic(15) in a Small Cohort of Patients.
    Czakó M; Till Á; Szabó A; Ripszám R; Melegh B; Hadzsiev K
    Int J Mol Sci; 2019 Oct; 20(19):. PubMed ID: 31590400
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Acute lymphoblastic leukemia in a nine-year-old girl with isodicentric chromosome 15 syndrome.
    Antonucci R; Vacca N; Ghisu E; Acquaviva G; Cosmi C; Marinaro AM; Locci C; Fozza C
    Cancer Genet; 2019 Jun; 235-236():93-94. PubMed ID: 31155481
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Small supernumerary marker chromosome 15 and a ring chromosome 15 associated with a 15q26.3 deletion excluding the IGF1R gene.
    Szabó A; Czakó M; Hadzsiev K; Duga B; Bánfai Z; Komlósi K; Melegh B
    Am J Med Genet A; 2018 Feb; 176(2):443-449. PubMed ID: 29226546
    [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. Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotype.
    Szabo A; Czako M; Hadzsiev K; Duga B; Komlosi K; Melegh B
    Mol Cytogenet; 2015; 8():41. PubMed ID: 26110020
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. The behavioral phenotype of the idic(15) syndrome.
    Battaglia A; Parrini B; Tancredi R
    Am J Med Genet C Semin Med Genet; 2010 Nov; 154C(4):448-55. PubMed ID: 20981774
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.
    Miller DT; Shen Y; Weiss LA; Korn J; Anselm I; Bridgemohan C; Cox GF; Dickinson H; Gentile J; Harris DJ; Hegde V; Hundley R; Khwaja O; Kothare S; Luedke C; Nasir R; Poduri A; Prasad K; Raffalli P; Reinhard A; Smith SE; Sobeih MM; Soul JS; Stoler J; Takeoka M; Tan WH; Thakuria J; Wolff R; Yusupov R; Gusella JF; Daly MJ; Wu BL
    J Med Genet; 2009 Apr; 46(4):242-8. PubMed ID: 18805830
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome.
    Chen CP; Lin SP; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):728-732. PubMed ID: 27751425
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Autistic symptoms among children and young adults with isodicentric chromosome 15.
    Rineer S; Finucane B; Simon EW
    Am J Med Genet; 1998 Sep; 81(5):428-33. PubMed ID: 9754629
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations.
    Sahoo T; Bacino CA; German JR; Shaw CA; Bird LM; Kimonis V; Anselm I; Waisbren S; Beaudet AL; Peters SU
    Eur J Hum Genet; 2007 Sep; 15(9):943-9. PubMed ID: 17522620
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder.
    Battaglia A
    Brain Dev; 2005 Aug; 27(5):365-9. PubMed ID: 16023554
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Three probands with autistic disorder and isodicentric chromosome 15.
    Wolpert CM; Menold MM; Bass MP; Qumsiyeh MB; Donnelly SL; Ravan SA; Vance JM; Gilbert JR; Abramson RK; Wright HH; Cuccaro ML; Pericak-Vance MA
    Am J Med Genet; 2000 Jun; 96(3):365-72. PubMed ID: 10898916
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel mechanisms of gene disruption at the medulloblastoma isodicentric 17p11 breakpoint.
    McCabe MG; Ichimura K; Pearson DM; Liu L; Clifford SC; Ellison DW; Collins VP
    Genes Chromosomes Cancer; 2009 Feb; 48(2):121-31. PubMed ID: 18973140
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Familial Small Supernumerary Marker Chromosome 15 Associated with Cryptic Mosaicism with Two Different Additional Marker Chromosomes Derived de novo from Chromosome 9: Detailed Case Study and Implications for Recurrent Pregnancy Loss.
    Čulić V; Lasan-Trcić R; Liehr T; Lebedev IN; Pivić M; Pavelic J; Vulić R
    Cytogenet Genome Res; 2018; 156(4):179-184. PubMed ID: 30466092
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A case of isodicentric chromosome 15 presented with epilepsy and developmental delay.
    Kim JS; Park J; Min BJ; Oh SK; Choi JS; Woo MJ; Chae JH; Kim KJ; Hwang YS; Lim BC
    Korean J Pediatr; 2012 Dec; 55(12):487-90. PubMed ID: 23300505
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mortality in isodicentric chromosome 15 syndrome: The role of SUDEP.
    Friedman D; Thaler A; Thaler J; Rai S; Cook E; Schanen C; Devinsky O
    Epilepsy Behav; 2016 Aug; 61():1-5. PubMed ID: 27218684
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes.
    Huang B; Crolla JA; Christian SL; Wolf-Ledbetter ME; Macha ME; Papenhausen PN; Ledbetter DH
    Hum Genet; 1997 Jan; 99(1):11-7. PubMed ID: 9003485
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.