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 *

265 related articles for article (PubMed ID: 8166428)

  • 1. A case of de novo translocation 7; 10 and the duplication 7p, deletion 10p phenotype.
    Park JP; McDermet MK; Moeschler JB; Wurster-Hill DH
    Ann Genet; 1993; 36(4):217-20. PubMed ID: 8166428
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Duplication of distal 22q.
    Abeliovich D; Maor E; Bashan N; Carmi R
    Am J Med Genet; 1989 Mar; 32(3):346-9. PubMed ID: 2729354
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A report of a patient with duplication of 7p13-->pter and deletion of 2p23-->pter due to a maternal 2p;7p translocation.
    Türköver BB; Sayar C; Toksoy G; Elçioğlu N
    Turk J Pediatr; 2009; 51(2):174-9. PubMed ID: 19480332
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Submicroscopic unbalanced translocation resulting in del10p/dup13q detected by subtelomere FISH.
    Roos A; Rudnik-Schöneborn S; Eggermann K; Eggermann T; Senderek J; Schwanitz G; Zerres K; Schüler HM
    Eur J Med Genet; 2006; 49(6):505-10. PubMed ID: 16905374
    [TBL] [Abstract][Full Text] [Related]  

  • 5. De novo concurrent 5p deletion and distal 17q duplication identified by fluorescence in situ hybridization (FISH).
    Szego K; Rauer M; Baratta E; Hoo JJ
    Ann Genet; 1993; 36(4):224-7. PubMed ID: 8166430
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Duplication of 7p21.2-->pter due to maternal 7p;21q translocation: implications for critical segment assignment in the 7p duplication syndrome.
    Cai T; Yu P; Tagle DA; Xia J
    Am J Med Genet; 1999 Oct; 86(4):305-11. PubMed ID: 10494083
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Trisomy of the short arm of chromosome 10p; description of a female patient with de novo duplication 10p11.2-15].
    Fechtrup B; Kalhoff H; Diekmann L; Fritz B
    Klin Padiatr; 2000; 212(1):35-40. PubMed ID: 10719682
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Partial trisomy 3p and partial monosomy 11q associated with atrial septal defect, cleft palate, and developmental delay: a case report.
    Tan EC; Lim E; Cham B; Knight L; Ng I
    Cytogenet Genome Res; 2011; 134(4):319-24. PubMed ID: 21654159
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.
    Courtens W; Wuyts W; Scheers S; Van Luijk R; Reyniers E; Rooms L; Ceulemans B; Kooy F; Wauters J
    Eur J Med Genet; 2006; 49(5):402-13. PubMed ID: 16488200
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Report of two cases of distal deletion of the long arm of chromosome 6.
    Stevens CA; Fineman RM; Breg WR; Silken AB
    Am J Med Genet; 1988 Apr; 29(4):807-14. PubMed ID: 3400725
    [TBL] [Abstract][Full Text] [Related]  

  • 11. De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome?
    Redha MA; Krishna Murthy DS; al-Awadi SA; al-Sulaiman IS; Sabry MA; el-Bahey SA; Farag TI
    Ann Genet; 1996; 39(1):5-9. PubMed ID: 9297445
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly.
    Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Hsu CY; Wu PC; Town DD; Lee DJ; Ma GC; Wang W
    Taiwan J Obstet Gynecol; 2010 Sep; 49(3):320-6. PubMed ID: 21056318
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
    Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
    Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Unbalanced three-way chromosomal translocation leading to deletion 18q and duplication 20p.
    Oegema R; van Zutven LJ; van Hassel DA; Huijbregts GC; Hoogeboom AJ
    Eur J Med Genet; 2012 Apr; 55(4):265-8. PubMed ID: 22406089
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
    de Ravel T; Aerssens P; Vermeesch JR; Fryns JP
    Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232
    [TBL] [Abstract][Full Text] [Related]  

  • 16. New chromosome aberration: duplication of a large part of chromosome 4q and partial deletion of chromosome 1q.
    Merlob P; Kohn G; Litwin A; Nissenkorn I; Katznelson MB; Reisner SH
    Am J Med Genet; 1989 Jan; 32(1):22-6. PubMed ID: 2705479
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Unbalanced translocation 46,XY,-15,+der(22)t(15;22)(q13;q11)pat: case report and review of the literature.
    Van Hove JL; McConkie-Rosell A; Chen YT; Iafolla AK; Lanman JT; Hennessy MD; Kahler SG
    Am J Med Genet; 1992 Sep; 44(1):24-30. PubMed ID: 1519645
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Small inherited terminal duplication of 7q with hydrocephalus, cleft palate, joint contractures, and severe hypotonia.
    Morava E; Bartsch O; Czakó M; Frensel A; Kalscheuer V; Kárteszi J; Kosztolányi G
    Clin Dysmorphol; 2003 Apr; 12(2):123-7. PubMed ID: 12868476
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Syndromal frontonasal dysostosis in a child with a complex translocation involving chromosomes 3, 7, and 11.
    Stevens CA; Qumsiyeh MB
    Am J Med Genet; 1995 Feb; 55(4):494-7. PubMed ID: 7762593
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
    Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.