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 *

224 related articles for article (PubMed ID: 26349184)

  • 21. A rare case of trisomy 11q23.3-11q25 and trisomy 22q11.1-22q11.21.
    Zou PS; Li HF; Chen LS; Ma M; Chen XH; Xue D; Cao DH
    Genet Mol Res; 2016 May; 15(2):. PubMed ID: 27173335
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Detection of a cryptic translocation t(13;20)(q34;p13) in an unexplained case of MCA/MR: value of FISH over high resolution banding.
    de Die-Smulders CE; Engelen JJ; Albrechts JC; Hamers GJ
    Am J Med Genet; 1999 Oct; 86(4):385-8. PubMed ID: 10494096
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cytogenomic characterization of an unexpected 17.6 Mb 9p deletion associated to a 14.8 Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotype.
    Meloni Vde F; Piazzon FB; Soares Mde F; Takeno SS; Christofolini DM; Kulikowski LD; Brunoni D; Melaragno MI
    Gene; 2012 Mar; 496(1):59-62. PubMed ID: 22285927
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Trisomy 7p resulting from isochromosome formation and whole-arm translocation.
    Lurie IW; Schwartz MF; Schwartz S; Cohen MM
    Am J Med Genet; 1995 Jan; 55(1):62-6. PubMed ID: 7702099
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Precocious puberty associated with partial trisomy 18q and monosomy 11q.
    Mutesa L; Hellin AC; Jamar M; Pierquin G; Bours V; Verloes A
    Genet Couns; 2007; 18(2):201-7. PubMed ID: 17710872
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Clinical and molecular characterization of chromosome 7p22.1 microduplication detected by array CGH.
    Chui JV; Weisfeld-Adams JD; Tepperberg J; Mehta L
    Am J Med Genet A; 2011 Oct; 155A(10):2508-11. PubMed ID: 21998864
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Subtelomeric rearrangements in Polish subjects with intellectual disability and dysmorphic features.
    Bogdanowicz J; Pawłowska B; Ilnicka A; Gawlik-Zawiślak S; Jóźwiak A; Sobiczewska B; Zdzienicka E; Korniszewski L; Zaremba J
    J Appl Genet; 2010; 51(2):215-7. PubMed ID: 20453310
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal diagnosis of a fetus with partial trisomy 7p.
    Ozgun MT; Batukan C; Basbug M; Akgun H; Caglayan O; Dundar M
    Fetal Diagn Ther; 2007; 22(3):229-32. PubMed ID: 17228165
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Direct duplication 16q11.1----16q13 is not associated with a typical dysmorphic syndrome.
    Fryns JP; Kleczkowska A; Decock P; Van den Berghe H
    Ann Genet; 1990; 33(1):46-8. PubMed ID: 2195981
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Brief report. Adult patient presenting an interstitial (9) (q21.32q31.1) direct duplication resulting from the malsegregation of a paternal balanced insertional translocation.
    Deng L; Peng Y; Liu J; Wen J; Xia Y; Liang D; Wu L
    Birth Defects Res A Clin Mol Teratol; 2014 Apr; 100(4):294-9. PubMed ID: 24668944
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization.
    Freitas ÉL; Gribble SM; Simioni M; Vieira TP; Silva-Grecco RL; Balarin MA; Prigmore E; Krepischi-Santos AC; Rosenberg C; Szuhai K; van Haeringen A; Carter NP; Gil-da-Silva-Lopes VL
    Am J Med Genet A; 2011 Nov; 155A(11):2754-61. PubMed ID: 21948691
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Duplication 7p in a family with t(7;11): association with anomalies of the anterior cranial base.
    Odell JM; Siebert JR; Bradley C; Salk D
    Am J Med Genet; 1987 Jul; 27(3):687-92. PubMed ID: 3631140
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Trisomy 20q caused by der(4) t(4;20) (q35;q13.1): report of a new patient and review of the literature.
    Plotner PL; Smith JL; Northrup H
    Am J Med Genet; 2002 Jul; 111(1):71-5. PubMed ID: 12124739
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Familial subtelomeric abnormality der(4)t(4p16.3;21q22.3) as a cause of mental retardation and mild dysmorphic features].
    Obersztyn E; Klapecki J; Helias-Rodzewicz Z; Bocian E; Mazurczak T
    Med Wieku Rozwoj; 2006; 10(1 Pt 2):199-209. PubMed ID: 17028389
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
    Sohn YB; Yun JN; Park SJ; Park MS; Kim SH; Lee JH
    Ann Clin Lab Sci; 2013; 43(3):332-6. PubMed ID: 23884231
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Familial distal monosomy 3p26.3-pter with trisomy 4q32.2-qter, presenting with progressive ataxia, intellectual disability, and dysmorphic features.
    Petriczko E; Biczysko-Mokosa A; Bogdanowicz J; Constantinou M; Zdziennicka E; Horodnicka-Jozwa A; Barg E; Gawlik-Zawislak S; Sulek-Piatkowska A; Dawid G; Walczak M; Pesz K; Kedzia A; Zajaczek S
    Am J Med Genet A; 2012 Jun; 158A(6):1442-6. PubMed ID: 22581569
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Chromosome 7 short arm deletion, 7p21----pter.
    Schömig-Spingler M; Schmid M; Brosi W; Grimm T
    Hum Genet; 1986 Nov; 74(3):323-5. PubMed ID: 3781561
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A case of insertional translocation resulting in partial trisomy 16p.
    Kokalj-Vokac N; Medica I; Zagorac A; Zagradisnik B; Erjavec A; Gregoric A
    Ann Genet; 2000; 43(3-4):131-5. PubMed ID: 11164194
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Trisomy 20q13 --> 20qter in a girl with multiple congenital malformations and a recombinant chromosome 20 inherited from a paternal inversion (20)(p13q13.1): clinical report and review of the trisomy 20q phenotype.
    Grange DK; Garcia-Heras J; Kilani RA; Lamp S
    Am J Med Genet A; 2005 Sep; 137A(3):308-12. PubMed ID: 16092120
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.