BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

124 related articles for article (PubMed ID: 10674160)

  • 1. Cerebellar dysgenesis and mental retardation associated with a complex chromosome rearrangement.
    Maserati E; Verri A; Seghezzi L; Tupler R; Federico A; Tiepolo L; Maraschio P
    Ann Genet; 1999; 42(4):210-4. PubMed ID: 10674160
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16.
    Phelan MC; Blackburn W; Rogers RC; Crawford EC; Cooley NR; Schrock E; Ning Y; Ried T
    Prenat Diagn; 1998 Nov; 18(11):1174-80. PubMed ID: 9854728
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mental retardation, tall stature and minor phenotypic abnormalities associated with a de novo complex chromosome rearrangement.
    De Brasi D; Della Casa R; Titomanlio L; D'Agostino A; Perone L; Andria G
    Neuropediatrics; 2000 Jun; 31(3):164-6. PubMed ID: 10963108
    [No Abstract]   [Full Text] [Related]  

  • 5. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient.
    Ballarati L; Recalcati MP; Bedeschi MF; Lalatta F; Valtorta C; Bellini M; Finelli P; Larizza L; Giardino D
    Eur J Med Genet; 2009; 52(4):218-23. PubMed ID: 19236961
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Complex chromosome rearrangement in a retarded girl with malformations.
    Kitsiou S; Tsezou A; Bartsocas CS; Tapratzi P; Kourakis G; Papas C; Dellagrammaticas H
    Ann Genet; 1987; 30(1):59-61. PubMed ID: 3498433
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features.
    Haddad MR; Mignon-Ravix C; Cacciagli P; Mégarbané A; Villard L
    Eur J Med Genet; 2009; 52(4):211-7. PubMed ID: 19379847
    [TBL] [Abstract][Full Text] [Related]  

  • 8. De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder.
    Goumy C; Mihaescu M; Tchirkov A; Giollant M; Benier C; Francannet C; Jaffray JY; Geneix A; Vago P
    Genet Couns; 2006; 17(3):371-9. PubMed ID: 17100206
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Balanced complex chromosomal rearrangements with more than four breakpoints: report of a new case.
    Till M; Devillard F; Crost P; Bachy M; Prieur F; Berthéas MF
    Am J Med Genet; 1991 Sep; 40(3):370-3. PubMed ID: 1951445
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A 6Mb deletion in band 2q22 due to a complex chromosome rearrangement associated with severe psychomotor retardation, microcephaly and distinctive dysmorphic facial features.
    Hoffer MJ; Hilhorst-Hofstee Y; Knijnenburg J; Hansson KB; Engelberts AC; Laan LA; Bakker E; Rosenberg C
    Eur J Med Genet; 2007; 50(2):149-54. PubMed ID: 17223398
    [TBL] [Abstract][Full Text] [Related]  

  • 11. De novo complex chromosome rearrangement: a study of two patients.
    Melo DG; Huber J; Giuliani LR; Mazzucatto LF; Riegel M; Pina-Neto JM
    Genet Couns; 2004; 15(3):303-10. PubMed ID: 15517822
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Duplication 16q12.1-q22.1 characterized by array CGH in a girl with spina bifida.
    Gustavsson P; Schoumans J; Staaf J; Borg A; Nordenskjöld M; Annerén G
    Eur J Med Genet; 2007; 50(3):237-41. PubMed ID: 17387046
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes.
    Bacino CA; Kashork CD; Davino NA; Shaffer LG
    Am J Med Genet; 2000 Jun; 92(4):250-5. PubMed ID: 10842290
    [TBL] [Abstract][Full Text] [Related]  

  • 14. De novo apparently balanced complex chromosome rearrangement (CCR) involving chromosomes 4, 18, and 21 in a girl with mental retardation: report and review.
    Batanian JR; Eswara MS
    Am J Med Genet; 1998 Jun; 78(1):44-51. PubMed ID: 9637422
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping.
    Peschka B; Leygraaf J; Hansmann D; Hansmann M; Schröck E; Ried T; Engels H; Schwanitz G; Schubert R
    Prenat Diagn; 1999 Dec; 19(12):1143-9. PubMed ID: 10590433
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Duplication of chromosome region (16)(p11.2 --> p12.1) in a mother and daughter with mild mental retardation.
    Engelen JJ; de Die-Smulders CE; Dirckx R; Verhoeven WM; Tuinier S; Curfs LM; Hamers AJ
    Am J Med Genet; 2002 Apr; 109(2):149-53. PubMed ID: 11977164
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Molecular cytogenetic analysis for a familial complex chromosomal rearrangement].
    Qian WP; Tan YQ; Tjia WM; Song D; Guan XY; Lu GX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun; 22(3):302-4. PubMed ID: 15952121
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Primary amenorrhea in a woman with a cryptic complex chromosome rearrangement involving the critical regions Xp11.2 and Xq24.
    Hernando C; Plaja A; Català V; Sarret E; Egozcue J; Fuster C
    Fertil Steril; 2004 Dec; 82(6):1666-71. PubMed ID: 15589876
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chromosomal aberrations evaluated by CGH, FISH and GTG-banding in a case of AIDS-related Burkitt's lymphoma.
    Zunino A; Viaggi S; Ottaggio L; Fronza G; Schenone A; Roncella S; Abbondandolo A
    Haematologica; 2000 Mar; 85(3):250-5. PubMed ID: 10702812
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification.
    Guilherme RS; Cernach MC; Sfakianakis TE; Takeno SS; Nardozza LM; Rossi C; Bhatt SS; Liehr T; Melaragno MI
    Cytogenet Genome Res; 2013; 141(4):317-23. PubMed ID: 23817307
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.