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 *

153 related articles for article (PubMed ID: 29441129)

  • 1. Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature.
    Li H; Du J; Li W; Cheng D; He W; Yi D; Xiong B; Yuan S; Tu C; Meng L; Luo A; Lin G; Lu G; Tan YQ
    Mol Cytogenet; 2018; 11():15. PubMed ID: 29441129
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The inv dup (15) or idic (15) syndrome (Tetrasomy 15q).
    Battaglia A
    Orphanet J Rare Dis; 2008 Nov; 3():30. PubMed ID: 19019226
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder.
    Lu Y; Liang Y; Ning S; Deng G; Xie Y; Song J; Zuo N; Feng C; Qin Y
    Mol Cytogenet; 2020; 13():21. PubMed ID: 32536972
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature.
    Chen CP; Lin CC; Li YC; Chern SR; Lee CC; Chen WL; Lee MS; Wang W; Tzen CY
    Prenat Diagn; 2004 Oct; 24(10):767-73. PubMed ID: 15503270
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. A study of two Chinese patients with tetrasomy and pentasomy 15q11q13 including Prader-Willi/Angelman syndrome critical region present with developmental delays and mental impairment.
    Yang J; Yang Y; Huang Y; Hu Y; Chen X; Sun H; Lv Z; Cheng Q; Bao L
    BMC Med Genet; 2013 Jan; 14():9. PubMed ID: 23320815
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Array-based comparative genomic hybridization analysis of recurrent chromosome 15q rearrangements.
    Sahoo T; Shaw CA; Young AS; Whitehouse NL; Schroer RJ; Stevenson RE; Beaudet AL
    Am J Med Genet A; 2005 Dec; 139A(2):106-13. PubMed ID: 16284940
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Double supernumerary isodicentric chromosomes derived from 15 resulting in partial hexasomy.
    Qumsiyeh MB; Rafi SK; Sarri C; Grigoriadou M; Gyftodimou J; Pandelia E; Laskari H; Petersen MB
    Am J Med Genet A; 2003 Feb; 116A(4):356-9. PubMed ID: 12522791
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Supernumerary tricentric derivative chromosome 15 in two boys with intractable epilepsy: another mechanism for partial hexasomy.
    Mann SM; Wang NJ; Liu DH; Wang L; Schultz RA; Dorrani N; Sigman M; Schanen NC
    Hum Genet; 2004 Jul; 115(2):104-11. PubMed ID: 15141347
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. [Genetic analysis of a case with mosaicism of a small supernumerary marker chromosome derived from idic(15)].
    Shao M; Wang Y; Zhao N; Liu P
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Jan; 39(1):85-88. PubMed ID: 34964975
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Complex small supernumerary marker chromosome with a 15q/16p duplication: clinical implications.
    Christofolini DM; Piazzon FB; Evo C; Mafra FA; Cosenza SR; Dias AT; Barbosa CP; Bianco B; Kulikowski LD
    Mol Cytogenet; 2014; 7():29. PubMed ID: 24839463
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

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

    [Next]    [New Search]
    of 8.