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 *

107 related articles for article (PubMed ID: 2758689)

  • 1. A case of de novo trisomy 12p syndrome.
    Tayel S; McCorquodale MM; Rutherford T; Kurczynski TW; Abdel-Aziz AM; el-Gabaldy F; Sharaf EA
    Clin Genet; 1989 May; 35(5):382-6. PubMed ID: 2758689
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Trisomy 12p syndrome: de novo occurrence of mosaic trisomy 12p in a mentally retarded boy.
    Kondo I; Hamaguchi H; Haneda T
    Hum Genet; 1979 Jan; 46(2):135-40. PubMed ID: 422196
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical and molecular cytogenetic observations in three cases of "trisomy 12p syndrome".
    Rauch A; Trautmann U; Pfeiffer RA
    Am J Med Genet; 1996 May; 63(1):243-9. PubMed ID: 8723117
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A case of de novo trisomy 12p syndrome.
    Ray M; Chudley AE; Christie N; Seargeant L
    Ann Genet; 1985; 28(4):235-8. PubMed ID: 3879436
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cytogenetic and molecular analysis in trisomy 12p.
    Allen TL; Brothman AR; Carey JC; Chance PF
    Am J Med Genet; 1996 May; 63(1):250-6. PubMed ID: 8723118
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Trisomy 12p and monosomy 4p: phenotype-genotype correlation.
    Benussi DG; Costa P; Zollino M; Murdolo M; Petix V; Carrozzi M; Pecile V
    Genet Test Mol Biomarkers; 2009 Apr; 13(2):199-204. PubMed ID: 19378504
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical, cytogenetic, and molecular characterization of a girl with some clinical features of Down syndrome resulting from a pure partial trisomy 21q22.11-qter due to a de novo intrachromosomal duplication.
    Vaglio A; Milunsky A; Quadrelli A; Huang XL; Maher T; Mechoso B; Martínez S; Pagano S; Bellini S; Costabel M; Quadrelli R
    Genet Test Mol Biomarkers; 2010 Feb; 14(1):57-65. PubMed ID: 20143912
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A case of de novo i(12p) with 12q whole-arm translocation mosaicism.
    Marques-de-Faria AP; Hackel C
    Am J Med Genet; 1989 Aug; 33(4):453-6. PubMed ID: 2596503
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Trisomy 12p syndrome. Evaluation of a family with a t(12;21) (p12.1;p11) translocation with unbalanced offspring.
    Hansteen IL; Schirmer L; Hestetun S
    Clin Genet; 1978 Apr; 13(4):339-49. PubMed ID: 148983
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Trisomy 12p mosaicism syndrome.
    Karki CB; Walters RM
    J Ment Defic Res; 1990 Feb; 34 ( Pt 1)():75-80. PubMed ID: 2139132
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3.
    Pfeiffer RA; Legat G; Trautmann U
    Ann Genet; 1992; 35(1):41-6. PubMed ID: 1610119
    [TBL] [Abstract][Full Text] [Related]  

  • 12. De novo inverted tandem duplication of the short arm of chromosome 12 in a patient with microblepharon.
    Tekin M; Jackson-Cook C; Pandya A
    Am J Med Genet; 2001 Nov; 104(1):42-6. PubMed ID: 11746026
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Report on 3 patients with 12p duplication including GRIN2B.
    Poirsier C; Landais E; Bednarek N; Nobecourt JM; Khoury M; Schmidt P; Morville P; Gruson N; Clomes S; Michel N; Riot A; Manjeongean C; Gaillard D; Doco-Fenzy M
    Eur J Med Genet; 2014 Apr; 57(5):185-94. PubMed ID: 24503147
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. De novostructural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies.
    Dufke A; Singer S; Borell-Kost S; Stotter M; Pflumm DA; Mau-Holzmann UA; Starke H; Mrasek K; Enders H
    Cytogenet Genome Res; 2006; 114(3-4):342-50. PubMed ID: 16954677
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndrome.
    Bijlsma JB; de France HF; Bleeker-Wagemakers LM; Dijkstra PF
    Hum Genet; 1978 Jan; 40(2):135-47. PubMed ID: 624544
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Tetrasomy for the short arm of chromosome 12 with accessory isochromosome (+i(12p)) and a marked LDH-B gene dosage effect.
    Steinbach P; Rehder H
    Clin Genet; 1987 Jul; 32(1):1-4. PubMed ID: 3476222
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Trisomy 12p syndrome: a chromosomal disorder associated with generalized 3-Hz spike and wave discharges.
    Guerrini R; Bureau M; Mattei MG; Battaglia A; Galland MC; Roger J
    Epilepsia; 1990; 31(5):557-66. PubMed ID: 2401247
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of the origin of a 22p+ chromosome by triplex dosage effect of LDH B, GAPHD, TPI and ENO2.
    Dallapiccola B; Brinchi V; Magnani M; Dacha M
    Ann Genet; 1980; 23(2):111-3. PubMed ID: 6967283
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Trisomy for the distal segment of the short arm of chromosome 17 in a boy with mild mental retardation and some dysmorphic features.
    Mégarbané A; Souraty N; Theophile D; Vekemans M; Samaras L; Ghorayeb Z
    Ann Genet; 1997; 40(1):55-9. PubMed ID: 9150851
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.