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 *

730 related articles for article (PubMed ID: 8488873)

  • 1. 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]  

  • 2. Two cases of 9p deletion syndrome and a case of partial trisomy 8 and partial monosomy 9p.
    Okten G; Sezer O; Günes S; Küçüködük S; Oğur G
    Genet Couns; 2009; 20(4):341-7. PubMed ID: 20162869
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH).
    Petty EM; Gibson LH; Breg WR; Burns JP; Yang-Feng TL
    Am J Med Genet; 1993 Mar; 45(6):770-3. PubMed ID: 8456860
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
    Chen CP; Su YN; Chern SR; Hsu CY; Tsai FJ; Wu PC; Lee CC; Chen YT; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2011 Mar; 50(1):67-73. PubMed ID: 21482378
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization.
    Guo WJ; Callif-Daley F; Zapata MC; Miller ME
    Am J Med Genet; 1995 Sep; 58(3):230-6. PubMed ID: 8533823
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Precise mapping of a de novo duplication 18(q21-->q22) utilizing cytogenetic, biochemical, and molecular techniques.
    Wolff DJ; Schwartz MF; Cohen MM; Schwartz S
    Am J Med Genet; 1993 Jun; 46(5):520-3. PubMed ID: 8322813
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Complex rearrangement involving 9p deletion and duplication in a syndromic patient: genotype/phenotype correlation and review of the literature.
    Recalcati MP; Bellini M; Norsa L; Ballarati L; Caselli R; Russo S; Larizza L; Giardino D
    Gene; 2012 Jul; 502(1):40-5. PubMed ID: 22537675
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [A case of 9p-syndrome identified chromosome 20 on chromosome 9p by M-FISH].
    Koseki N; Obara Y; Ookawa A; Katsumi M; Funato T; Kaku M
    Rinsho Byori; 2001 Oct; 49(10):1045-8. PubMed ID: 11769470
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
    Kobayashi J; Kimijima Y; Yamada S; Amagasa T; Saito-Ohara F
    J Craniomaxillofac Surg; 2000 Jun; 28(3):165-70. PubMed ID: 10964553
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Phenotypic and cytogenetic spectrum of 9p trisomy.
    Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
    Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
    Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A dysmorphic newborn with 45,X,der(1)inv(1)(p13;qter)t(Y;1)(pter-->q11;p13),-Y de novo karyotype.
    Tatar A; Oztas S; Yakut T; Ors R
    Genet Couns; 2005; 16(2):173-7. PubMed ID: 16080298
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridization.
    Zenger-Hain JL; Van Dyke DL; Wiktor A; Walker H; Feldman GL
    Am J Med Genet; 1993 Dec; 47(8):1198-201. PubMed ID: 8291556
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Complex familial rearrangement of chromosome 9p24.3 detected by FISH.
    Repetto GM; Wagstaff J; Korf BR; Knoll JH
    Am J Med Genet; 1998 Apr; 76(4):306-9. PubMed ID: 9545094
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Another rare case of a child with de novo terminal 9p deletion and co-existing interstitial 9p duplication: clinical findings and molecular cytogenetic study by array-CGH.
    Kowalczyk M; Tomaszewska A; Podbioł-Palenta A; Constantinou M; Wawrzkiewicz-Witkowska A; Kowalski J; Kałużewski B; Zajączek S; Srebniak MI
    Cytogenet Genome Res; 2013; 139(1):9-16. PubMed ID: 22965227
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Translocation/duplication of 9p onto a duplicated 4q.
    Rivera H; Figuera LE; Vasquez AI
    Genet Couns; 1992; 3(4):201-3. PubMed ID: 1472355
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
    Esmer MC; Carnevale A; Gómez L; del Castillo V; Frías S
    Rev Invest Clin; 1996; 48(1):27-33. PubMed ID: 8815483
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
    Spikes AS; Hegmann K; Smith JL; Shaffer LG
    Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patient.
    Lukusa T; Van Buggenhout G; Devriendt K; Fryns JP
    Genet Couns; 2002; 13(1):1-10. PubMed ID: 12017231
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 37.