BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

512 related articles for article (PubMed ID: 7573156)

  • 1. Partial trisomy 13q identified by sequential fluorescence in situ hybridization.
    Rao VV; Carpenter NJ; Gucsavas M; Coldwell J; Say B
    Am J Med Genet; 1995 Jul; 58(1):50-3. PubMed ID: 7573156
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
    Kímya Y; Yakut T; Egelí U; Ozerkan K
    Prenat Diagn; 2002 Nov; 22(11):957-61. PubMed ID: 12424755
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Maternal origin of extra marker chromosome 1Q31.1-qter and 13pter-q12.12 in a child with dysmorhic features.
    Rao VB; Kerketta L; Korgaonkar S; Ghosh K; Mohanty D
    Genet Couns; 2005; 16(2):139-43. PubMed ID: 16082769
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
    Lukusa T; van den Berghe L; Smeets E; Fryns JP
    Ann Genet; 1999; 42(4):215-20. PubMed ID: 10674161
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
    DuPont BR; Huff RW; Ridgway LE; Stratton RF; Moore CM
    Am J Med Genet; 1994 Mar; 50(1):21-7. PubMed ID: 8160748
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
    Chen CP; Chern SR; Lin CC; Wang TH; Li YC; Hsieh LJ; Lee CC; Hua HM; Wang W
    Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
    Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E
    J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Trisomy of 8q22.3 approximately q23-qter following an unbalanced 1;8 translocation in a boy with multiple anomalies.
    Ergun MA; Balci S; Konaç E; Kan D; Menevşe S; Bartsch O
    Turk J Pediatr; 2004; 46(4):384-7. PubMed ID: 15641279
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial trisomy 8p (8p11.2-->pTER) and deletion of 13q (13q32-->qTER): case report.
    Yeşilyurt A; Dilli D; Oguz S; Dilmen U; Altug N; Candemir Z
    Genet Couns; 2011; 22(1):35-40. PubMed ID: 21614986
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Confirmation of proximal 1q duplication using fluorescence in situ hybridization.
    Chen H; Kusyk CJ; Tuck-Muller CM; Martinez JE; Dorand RD; Wertelecki W
    Am J Med Genet; 1994 Mar; 50(1):28-31. PubMed ID: 8160749
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS; Kamel AK; Helmy NA
    Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A partial trisomy 15q due to 15;17 translocation detected by conventional cytogenetic and FISH techniques.
    Cora T; Acar H; Oran B
    Genet Couns; 2000; 11(1):25-32. PubMed ID: 10756424
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Atypical 18p- syndrome associated with partial trisomy 16p in a chromosomally unbalanced child of consanguineous parents with an identical balanced translocation.
    Kupchik GS; Barrett SK; Babu A; Charria-Ortiz G; Velinov M; Macera MJ
    Eur J Med Genet; 2005; 48(1):57-65. PubMed ID: 15953407
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotype.
    Mach M; Windpassinger C; Wagner K; Kroisel PM; Petek E
    Genet Couns; 2007; 18(1):9-16. PubMed ID: 17515297
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Partial trisomy 1 with congenital hydrocephalus and hypogammaglobulinemia: report of one case.
    Hwu WL; Kuo PL; Hung YT; Chien YH; Chu SY
    Acta Paediatr Taiwan; 2004; 45(2):97-9. PubMed ID: 15335120
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
    Hegmann KM; Spikes AS; Orr-Urtreger A; Shaffer LG
    Am J Med Genet; 1996 Jan; 61(1):10-5. PubMed ID: 8741910
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report.
    Mundhofir FE; Kooper AJ; Winarni TI; Smits AP; Faradz SM; Hamel BC
    Genet Couns; 2010; 21(1):99-108. PubMed ID: 20420036
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Constitutional partial 1q trisomy mosaicism and Wilms tumor.
    Mark HF; Wyandt H; Pan A; Milunsky JM
    Cancer Genet Cytogenet; 2005 Oct; 162(2):166-71. PubMed ID: 16213366
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Detection of an unbalanced t(4;15) by FISH in a child with multiple congenital anomalies.
    Celep F; Acar H; Aynaci O; Aynaci FM; Karagüzel A
    Genet Couns; 2001; 12(4):319-26. PubMed ID: 11837600
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 26.