BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

174 related articles for article (PubMed ID: 9021016)

  • 1. Delineation of a duplication map of chromosome 3q: a new case confirms the exclusion of 3q25-q26.2 from the duplication 3q syndrome critical region.
    Rizzu P; Haddad BR; Vallcorba I; Alonso A; Ferro MT; Garcia-Sagredo JM; Baldini A
    Am J Med Genet; 1997 Feb; 68(4):428-32. PubMed ID: 9021016
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Partial duplication of 3q (q25.1-->q26.1) without the Brachmann-de Lange phenotype.
    Lopez-Rangel E; Dill FJ; Hrynchak MA; Van Allen MI
    Am J Med Genet; 1993 Nov; 47(7):1068-71. PubMed ID: 8291525
    [TBL] [Abstract][Full Text] [Related]  

  • 3. First report of a partial trisomy 3q12-q23 de novo--FISH breakpoint determination and phenotypic characterization.
    Gamerdinger U; Bosse K; Eggermann T; Kalscheuer V; Schwanitz G; Engels H
    Eur J Med Genet; 2006; 49(3):225-34. PubMed ID: 16762824
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Duplication 3q syndrome: molecular delineation of the critical region.
    Aqua MS; Rizzu P; Lindsay EA; Shaffer LG; Zackai EH; Overhauser J; Baldini A
    Am J Med Genet; 1995 Jan; 55(1):33-7. PubMed ID: 7702094
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype.
    Mewar R; Harrison W; Weaver DD; Palmer C; Davee MA; Overhauser J
    Am J Med Genet; 1994 Aug; 52(2):178-83. PubMed ID: 7802005
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A patient with an interstitial duplication of chromosome 5p11-p13.3 further confirming a critical region for 5p duplication syndrome.
    Loscalzo ML; Becker TA; Sutcliffe M
    Eur J Med Genet; 2008; 51(1):54-60. PubMed ID: 18006398
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new case of dup(3q) syndrome due to a pure duplication of 3qter.
    Faas BH; De Vries BB; Van Es-Van Gaal J; Merkx G; Draaisma JM; Smeets DF
    Clin Genet; 2002 Oct; 62(4):315-20. PubMed ID: 12372060
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.
    Wyandt HE; Shim SH; Mark HF; Huang XL; Milunsky JM
    Exp Mol Pathol; 2006 Jun; 80(3):262-6. PubMed ID: 16516886
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel case of dup(3q) syndrome due to a de novo interstitial duplication 3q24-q26.31 with minimal overlap to the dup(3q) critical region.
    Meins M; Hagh JK; Gerresheim F; Einhoff E; Olschewski H; Strehl H; Epplen JT
    Am J Med Genet A; 2005 Jan; 132A(1):84-9. PubMed ID: 15551338
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 17p11.2p12 triplication and del(17)q11.2q12 in a severely affected child with dup(17)p11.2p12 syndrome.
    Girirajan S; Williams S; Garbern J; Nowak N; Hatchwell E; Elsea S
    Clin Genet; 2007 Jul; 72(1):47-58. PubMed ID: 17594399
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Duplication 10q confirmed by DNA in situ hybridization.
    Johnson VP; Sutliff WC
    Am J Med Genet; 1994 Aug; 52(2):184-7. PubMed ID: 7802006
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Interstitial 6q duplication in an adult male without growth delay or severe mental retardation.
    Cappon SL; Duncan AM; Khalifa MM
    Med Sci Monit; 2000; 6(3):581-5. PubMed ID: 11208374
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial duplication of 4q12q13 leads to a mild phenotype.
    Shashi V; Berry MN; Santos C; Pettenati MJ
    Am J Med Genet; 1999 Sep; 86(1):51-3. PubMed ID: 10440828
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Subchromosomal band interval mapping and ordering of DNA markers in the region 3q26.3-q27 involved in the dup(3q) syndrome.
    Rizzu P; Baldini A
    Genomics; 1994 Dec; 24(3):580-2. PubMed ID: 7713511
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
    Peeters H; Vermeesch J; Fryns JP
    Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The dup(3q) syndrome: report of eight cases and review of the literature.
    Steinbach P; Adkins WN; Caspar H; Dumars KW; Gebauer J; Gilbert EF; Grimm T; Habedank M; Hansmann I; Herrmann J; Kaveggia EG; Langenbeck U; Meisner LF; Najafzadeh TM; Opitz JM; Palmer CG; Peters HH; Scholz W; Tavares AS; Wiedeking C
    Am J Med Genet; 1981; 10(2):159-77. PubMed ID: 7315873
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Direct duplication of 9p22-->p24 in a child with duplication 9p syndrome.
    Fujimoto A; Lin MS; Schwartz S
    Am J Med Genet; 1998 May; 77(4):268-71. PubMed ID: 9600733
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Two patients with overlapping de novo duplications of the long arm of chromosome 9, including one case with Di George sequence.
    Lindgren V; Rosinsky B; Chin J; Berry-Kravis E
    Am J Med Genet; 1994 Jan; 49(1):67-73. PubMed ID: 8172253
    [TBL] [Abstract][Full Text] [Related]  

  • 19. High resolution microarray CGH and MLPA analysis for improved genotype/phenotype evaluation of two childhood genetic disorder cases: ring chromosome 19 and partial duplication 2q.
    Hermsen MA; Tijssen M; Acero IH; Meijer GA; Ylstra B; Toral JF
    Eur J Med Genet; 2005; 48(3):310-8. PubMed ID: 16179226
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Further delineation of the dup(3q) syndrome.
    Wilson GN; Dasouki M; Barr M
    Am J Med Genet; 1985 Sep; 22(1):117-23. PubMed ID: 4050847
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.