BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 3499849)

  • 1. Dissociation of tdic chromosomes: about a t(15;18)(p11;p11) leading to 18p monosomy.
    Garcia-Esquivel L; Rivera H; Sanchez-Corona J; Ramirez ML; Jimenez M; Cantú JM
    Ann Genet; 1987; 30(2):94-7. PubMed ID: 3499849
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular cytogenetic characterization of 18;21 whole arm translocation associated with monosomy 18p.
    Wang JC; Nemana L; Kou SY; Habibian R; Hajianpour MJ
    Am J Med Genet; 1997 Sep; 71(4):463-6. PubMed ID: 9286456
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisation.
    Alkan M; Ramelli GP; Hirsiger H; Keser I; Remonda L; Bühler EM; Moser H
    Genet Couns; 2002; 13(2):151-6. PubMed ID: 12150215
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Keratosis pilaris and ulerythema ophryogenes associated with an 18p deletion caused by a Y/18 translocation.
    Nazarenko SA; Ostroverkhova NV; Vasiljeva EO; Nazarenko LP; Puzyrev VP; Malet P; Nemtseva TA
    Am J Med Genet; 1999 Jul; 85(2):179-82. PubMed ID: 10406673
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial monosomy 15q due to de novo t(15;22)(q15;p11).
    Mori MA; Rodriguez L; Pinel I; Casas JM; Diaz de Bustamante A; Martinez-Frias ML
    Ann Genet; 1987; 30(4):246-8. PubMed ID: 3322163
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin.
    Oner G; Jauch A; Eggermann T; Hardwick R; Kirsch S; Schiebel K; Rappold G; Robson L; Smith A
    Am J Med Genet; 2000 May; 92(2):101-6. PubMed ID: 10797432
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes.
    Tharapel AT; Qumsiyeh MB; Martens PR; Tharapel SA; Dalton JD; Ward JC; Wilroy RS
    Am J Med Genet; 1991 Jul; 40(1):117-20. PubMed ID: 1887840
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 18p monosomy with midline defects and a de novo satellite identified by FISH.
    Taine L; Goizet C; Wen ZQ; Chateil JF; Battin J; Saura R; Lacombe D
    Ann Genet; 1997; 40(3):158-63. PubMed ID: 9401105
    [TBL] [Abstract][Full Text] [Related]  

  • 9. De novo (15;21) unbalanced translocation of paternal origin in a girl with Prader-Willi syndrome.
    Cuoco C; Bicocchi MP; Granata D; Mezzano P; Serra G
    Am J Med Genet; 1990 Sep; 37(1):62-4. PubMed ID: 2240045
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion.
    Prontera P; Aiello V; Toschi M; Turci A; Gruppioni R; Buldrini B; Zago S; Bonfatti A; Donti E; Calzolari E; Sensi A
    Genet Couns; 2007; 18(3):309-15. PubMed ID: 18019372
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p.
    McGhee EM; Qu Y; Wohlferd MM; Goldberg JD; Norton ME; Cotter PD
    Clin Genet; 2001 Apr; 59(4):274-8. PubMed ID: 11298684
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Translocation (X;13)(p11.21;q12.3) in a girl with incontinentia pigmenti and bilateral retinoblastoma.
    Kajii T; Tsukahara M; Fukushima Y; Hata A; Matsuo K; Kuroki Y
    Ann Genet; 1985; 28(4):219-23. PubMed ID: 3879432
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Reciprocal translocation t(1;15)(p36.2;p11.2): confirmation of a suggestive cytogenetic diagnosis by in situ hybridization and clinical case report on resulting monosomy (1p).
    Barbi G; Kennerknecht I; Klett C
    Am J Med Genet; 1992 Jul; 43(4):722-5. PubMed ID: 1621764
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Use of chromosome painting for marker chromosome identification in two children with congenital disorders.
    Doco-Fenzy M; Navrocki B; Cornillet P; Sabouraud P; Robillard P; Gruson N; Gaillard D; Adnet JJ
    Bull Assoc Anat (Nancy); 1994 Jun; 78(241):9-13. PubMed ID: 8086666
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A new case of monosomy for 17q25----qter due to a maternal translocation [t(3;17)(p12;q24)].
    Luke S; Bennett HS; Pitter JH; Verma RS
    Ann Genet; 1992; 35(1):48-50. PubMed ID: 1610120
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A tdic(5;15)(p31;p11) chromosome showing variation for constriction in the centromeric regions in a patient with the cri du chat syndrome.
    Dewald GW; Boros SJ; Conroy MM; Dahl RJ; Spurbeck JL; Vitek HA
    Cytogenet Cell Genet; 1979; 24(1):15-26. PubMed ID: 456039
    [TBL] [Abstract][Full Text] [Related]  

  • 17. t(15;21)(q15;q22.1) pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring.
    Abeliovich D; Dagan J; Lerer I; Silberstein S; Katznelson MB; Frydman M
    Am J Med Genet; 1996 Dec; 66(1):45-51. PubMed ID: 8957510
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Duplication 18p with mild influence on the phenotype.
    Johansson B; Mertens F; Palm L; Englesson I; Kristoffersson U
    Am J Med Genet; 1988 Apr; 29(4):871-4. PubMed ID: 3400732
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Partial 9p monosomy in a girl with a tdic(9p23;13p11) translocation, minor anomalies, obesity, and mental retardation.
    Serra A; Bova R; Bellanova G; Chindemi A; Zappata S; Brahe C
    Am J Med Genet; 1997 Aug; 71(2):139-43. PubMed ID: 9217211
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Partial trisomy and monosomy 21 in an infant with an unusual de novo 21/21 translocation.
    Cantu JM; Hernandez A; Plascencia L; Vaca G; Moller M; Rivera H
    Ann Genet; 1980; 23(3):183-6. PubMed ID: 6448566
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.