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 *

121 related articles for article (PubMed ID: 16470730)

  • 1. Clinical findings in 33 subjects with large supernumerary marker(15) chromosomes and 3 subjects with triplication of 15q11-q13.
    Dennis NR; Veltman MW; Thompson R; Craig E; Bolton PF; Thomas NS
    Am J Med Genet A; 2006 Mar; 140(5):434-41. PubMed ID: 16470730
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexity.
    Roberts SE; Maggouta F; Thomas NS; Jacobs PA; Crolla JA
    Am J Hum Genet; 2003 Nov; 73(5):1061-72. PubMed ID: 14560400
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14.
    Ungaro P; Christian SL; Fantes JA; Mutirangura A; Black S; Reynolds J; Malcolm S; Dobyns WB; Ledbetter DH
    J Med Genet; 2001 Jan; 38(1):26-34. PubMed ID: 11134237
    [TBL] [Abstract][Full Text] [Related]  

  • 4. De novo interstitial duplication of the 15q11.2-q14 PWS/AS region of maternal origin: Clinical description, array CGH analysis, and review of the literature.
    Kitsiou-Tzeli S; Tzetis M; Sofocleous C; Vrettou C; Xaidara A; Giannikou K; Pampanos A; Mavrou A; Kanavakis E
    Am J Med Genet A; 2010 Aug; 152A(8):1925-32. PubMed ID: 20575009
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterisation of interstitial duplications and triplications of chromosome 15q11-q13.
    Roberts SE; Dennis NR; Browne CE; Willatt L; Woods G; Cross I; Jacobs PA; Thomas S
    Hum Genet; 2002 Mar; 110(3):227-34. PubMed ID: 11935334
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Partial hexasomy for the Prader-Willi-Angelman syndrome critical region due to a maternally inherited large supernumerary marker chromosome.
    Hoppman-Chaney NL; Dawson DB; Nguyen L; Sengupta S; Reynolds K; McPherson E; Velagaleti G
    Am J Med Genet A; 2010 Aug; 152A(8):2034-8. PubMed ID: 20602489
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Infantile spasms in a mosaic monocentric and duplicated SMC 15 patient.
    Isobe K; Matsumoto H; Tamura Y; Hashimoto J; Matsubara K; Nonoyama S
    Brain Dev; 2018 Nov; 40(10):891-896. PubMed ID: 29960745
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man.
    Guanciali-Franchi P; Calabrese G; Morizio E; Gatta V; Palka C; Stuppia L; Zuffardi O
    Eur J Med Genet; 2008; 51(3):239-44. PubMed ID: 18378203
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: case report.
    Kraoua L; Chaabouni M; Ewers E; Chelly I; Ouertani I; Ben Jemaa L; Maazoul F; Liehr T; Chaabouni H
    Eur J Med Genet; 2011; 54(4):e446-50. PubMed ID: 21621018
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Duplication of the 15q11-q13 region: clinical and genetic study of 30 new cases.
    Al Ageeli E; Drunat S; Delanoë C; Perrin L; Baumann C; Capri Y; Fabre-Teste J; Aboura A; Dupont C; Auvin S; El Khattabi L; Chantereau D; Moncla A; Tabet AC; Verloes A
    Eur J Med Genet; 2014 Jan; 57(1):5-14. PubMed ID: 24239951
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A patient with Prader-Willi syndrome and a supernumerary marker chromosome r(15)(q11.1-13p11.1)pat and maternal heterodisomy.
    Werner M; Ben-Neriah Z; Silverstein S; Lerer I; Dagan Y; Abeliovich D
    Am J Med Genet A; 2004 Aug; 129A(2):176-9. PubMed ID: 15316980
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Investigation of a cryptic interstitial duplication involving the Prader-Willi/Angelman syndrome critical region.
    Thomas NS; Browne CE; Oley C; Healey S; Crolla JA
    Hum Genet; 1999 Nov; 105(5):384-7. PubMed ID: 10598802
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage.
    Wang NJ; Liu D; Parokonny AS; Schanen NC
    Am J Hum Genet; 2004 Aug; 75(2):267-81. PubMed ID: 15197683
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in Taiwan.
    Hou JW; Wang TR
    Eur J Pediatr; 1998 Feb; 157(2):122-7. PubMed ID: 9504785
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. A case of mosaic supernumerary ring chromosome 15 with two copies of the segment 15p11.1-q14.
    Zou YS; McGrann PS; Uphoff TS; Van Dyke DL
    Am J Med Genet A; 2006 Aug; 140(15):1663-8. PubMed ID: 16830338
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Does parent of origin matter? Methylation studies should be performed on patients with multiple copies of the Prader-Willi/Angelman syndrome critical region.
    Aypar U; Brodersen PR; Lundquist PA; Dawson DB; Thorland EC; Hoppman N
    Am J Med Genet A; 2014 Oct; 164A(10):2514-20. PubMed ID: 24975781
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.