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 *

163 related articles for article (PubMed ID: 15225160)

  • 21. Small supernumerary marker chromosome derived from proximal p-arm of chromosome 2: identification by fluorescent in situ hybridization.
    Lasan Trcić R; Hitrec V; Letica L; Cuk M; Begović D
    Croat Med J; 2003 Aug; 44(4):477-9. PubMed ID: 12950153
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Molecular cytogenetic characterization of a small, familial supernumerary ring chromosome 7 associated with mental retardation and an abnormal phenotype.
    Tan-Sindhunata G; Castedo S; Leegte B; Mulder I; vd Veen AY; vd Hout AH; Wiersma TJ; van Essen AJ
    Am J Med Genet; 2000 May; 92(2):147-52. PubMed ID: 10797441
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Terminal deletion 2q37.3 in a patient with Klippel-Trenaunay-Weber syndrome.
    Puiu I; Stoica A; Sosoi S; Puiu A; Ioana M; Burada F
    Fetal Pediatr Pathol; 2013 Oct; 32(5):351-6. PubMed ID: 23438794
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Five cases of supernumerary small ring chromosomes 1: heterogeneity and genotype-phenotype correlation.
    Bernardini L; Capalbo A; D'Avanzo MG; Torrente I; Grammatico P; Dell'Edera D; Cavalcanti DP; Novelli A; Dallapiccola B
    Eur J Med Genet; 2007; 50(2):94-102. PubMed ID: 17236832
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Identification and characterization of a new type of asymmetrical dicentric chromosome derived from a single maternal chromosome 18.
    Lin CC; Li YC; Liu PP; Hsieh LJ; Cheng YM; Teng RH; Shi SL; Tsai FJ
    Cytogenet Genome Res; 2007; 119(3-4):291-6. PubMed ID: 18253044
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
    Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
    Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Small familial supernumerary ring chromosome 2: FISH characterization and genotype-phenotype correlation.
    Giardino D; Finelli P; Russo S; Gottardi G; Rodeschini O; Atza MG; Natacci F; Larizza L
    Am J Med Genet; 2002 Aug; 111(3):319-23. PubMed ID: 12210331
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.
    Chantot-Bastaraud S; Muti C; Pipiras E; Routon MC; Roubergue A; Burglen L; Siffroi JP; Simon-Bouy B
    Ann Genet; 2004; 47(3):241-9. PubMed ID: 15337469
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Characterization of a small supernumerary ring X chromosome by fluorescence in situ hybridization.
    Duncan AM; Macdonald A; Brown CJ; Wolff D; Willard HF; Sutton B
    Am J Med Genet; 1993 Dec; 47(8):1153-6. PubMed ID: 8291547
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A large analphoid invdup(3)(q22.3qter) marker chromosome characterized by array-CGH in a child with malformations, mental retardation, ambiguous genitalia and Blaschko's lines.
    Gimelli G; Giorda R; Beri S; Gimelli S; Zuffardi O
    Eur J Med Genet; 2007; 50(4):264-73. PubMed ID: 17567547
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Characterization of an analphoid, neocentromere-positive inv dup 8p marker chromosome using multiplex whole chromosome and sub-telomere FISH analyses.
    Velinov M; Gu H; Genovese M; Duncan C; Warburton P; Brooks SS; Jenkins EC
    Ann Genet; 2004; 47(2):199-205. PubMed ID: 15183754
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prenatal diagnosis of a de novo supernumerary marker derived from chromosome 16.
    Hengstschläger M; Bettelheim D; Drahonsky R; Deutinger J; Bernaschek G
    Prenat Diagn; 2001 Jun; 21(6):477-80. PubMed ID: 11438953
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Interstitial deletion 2p accompanied by marker chromosome formation of the deleted segment resulting in a stable acentric marker chromosome.
    Petit P; Fryns JP
    Genet Couns; 1997; 8(4):341-3. PubMed ID: 9457505
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Characterization of a supernumerary small marker X chromosome in two females with similar phenotypes.
    Tümer Z; Wolff D; Silahtaroglu AN; Orum A; Brøndum-Nielsen K
    Am J Med Genet; 1998 Feb; 76(1):45-50. PubMed ID: 9508064
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
    Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis.
    Li MM; Howard-Peebles PN; Killos LD; Fallon L; Listgarten E; Stanley WS
    Prenat Diagn; 2000 Feb; 20(2):138-43. PubMed ID: 10694686
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Midline defects in deletion 18p syndrome: clinical and molecular characterization of three patients.
    Portnoï MF; Gruchy N; Marlin S; Finkel L; Denoyelle F; Dubourg C; Odent S; Siffroi JP; Le Bouc Y; Houang M
    Clin Dysmorphol; 2007 Oct; 16(4):247-52. PubMed ID: 17786116
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Sturge--Weber-Klippel--Trenaunay syndrome (case report)].
    Rafai MA; Otmani HE; Boulaajaj FZ; Sibai M; Moutaouakkil F; Chlihi A; Slassi I
    J Mal Vasc; 2008 Feb; 33(1):35-8. PubMed ID: 18343067
    [TBL] [Abstract][Full Text] [Related]  

  • 39. FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22).
    Bartsch O; Rasi S; Hoffmann K; Blin N
    Eur J Hum Genet; 2005 May; 13(5):592-8. PubMed ID: 15756300
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Trisomy of medial 15q as result of an analphoid supernumerary ring chromosome detected by CGH and FISH.
    Constantinou M; Płowás I; Kałuzewski B
    Cytogenet Genome Res; 2007; 119(1-2):165-9. PubMed ID: 18160798
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.