BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

101 related articles for article (PubMed ID: 9860303)

  • 1. Neurofibromatosis pseudogene amplification underlies euchromatic cytogenetic duplications and triplications of proximal 15q.
    Barber JC; Cross IE; Douglas F; Nicholson JC; Moore KJ; Browne CE
    Hum Genet; 1998 Nov; 103(5):600-7. PubMed ID: 9860303
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic level.
    Barber JC; Reed CJ; Dahoun SP; Joyce CA
    Hum Genet; 1999 Mar; 104(3):211-8. PubMed ID: 10323244
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15q.
    Fantes JA; Mewborn SK; Lese CM; Hedrick J; Brown RL; Dyomin V; Chaganti RS; Christian SL; Ledbetter DH
    J Med Genet; 2002 Mar; 39(3):170-7. PubMed ID: 11897815
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Proximal 15q familial euchromatic variant and PWS/AS critical region duplication in the same patient: a cytogenetic pitfall.
    Carelle-Calmels N; Girard-Lemaire F; Guérin E; Bieth E; Rudolf G; Biancalana V; Pecheur H; Demil H; Schneider T; de Saint-Martin A; Caron O; Legrain M; Gaston V; Flori E
    Eur J Med Genet; 2008; 51(6):547-57. PubMed ID: 18692163
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Novel deletion variants of 9q13-q21.12 and classical euchromatic variants of 9q12/qh involve deletion, duplication and triplication of large tracts of segmentally duplicated pericentromeric euchromatin.
    Willatt LR; Barber JC; Clarkson A; Simonic I; Raymond FL; Docherty Z; Ogilvie CM
    Eur J Hum Genet; 2007 Jan; 15(1):45-52. PubMed ID: 16985501
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations.
    Browne CE; Dennis NR; Maher E; Long FL; Nicholson JC; Sillibourne J; Barber JC
    Am J Hum Genet; 1997 Dec; 61(6):1342-52. PubMed ID: 9399882
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inherited DNA amplification of the proximal 15q region: cytogenetic and molecular studies.
    Mignon C; Parente F; Stavropoulou C; Collignon P; Moncla A; Turc-Carel C; Mattei MG
    J Med Genet; 1997 Mar; 34(3):217-22. PubMed ID: 9132493
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A third neurofibromatosis type 1 (NF1) pseudogene at chromosome 15q11.2.
    Kehrer-Sawatzki H; Schwickardt T; Assum G; Rocchi M; Krone W
    Hum Genet; 1997 Oct; 100(5-6):595-600. PubMed ID: 9341878
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. A large polymorphic repeat in the pericentromeric region of human chromosome 15q contains three partial gene duplications.
    Ritchie RJ; Mattei MG; Lalande M
    Hum Mol Genet; 1998 Aug; 7(8):1253-60. PubMed ID: 9668167
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Analysis of 10 patients with duplications of 15q11q13 region and autism features].
    Wang W; Hu C; Bi X; Yuan H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Feb; 35(1):23-28. PubMed ID: 29419854
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26.
    Pujana MA; Nadal M; Gratacòs M; Peral B; Csiszar K; González-Sarmiento R; Sumoy L; Estivill X
    Genome Res; 2001 Jan; 11(1):98-111. PubMed ID: 11156619
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Characterization of an autism-associated segmental maternal heterodisomy of the chromosome 15q11-13 region.
    Kwasnicka-Crawford DA; Roberts W; Scherer SW
    J Autism Dev Disord; 2007 Apr; 37(4):694-702. PubMed ID: 17006779
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay.
    Mohandas TK; Park JP; Spellman RA; Filiano JJ; Mamourian AC; Hawk AB; Belloni DR; Noll WW; Moeschler JB
    Am J Med Genet; 1999 Feb; 82(4):294-300. PubMed ID: 10051161
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.