BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

245 related articles for article (PubMed ID: 15235171)

  • 1. Partial trisomy 13 with features similar to C syndrome.
    Phadke SR; Patil SJ
    Indian Pediatr; 2004 Jun; 41(6):614-7. PubMed ID: 15235171
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [Trisomy 13 syndrome, Patau syndrome].
    Tsukino R; Sasaki M
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):332-4. PubMed ID: 11057250
    [No Abstract]   [Full Text] [Related]  

  • 4. Kabuki syndrome and trisomy 10p.
    Utine GE; Alanay Y; Atkaş D; Boduroğlu K; Alikaşifoğlu M; Tunçbilek E
    Genet Couns; 2008; 19(3):291-300. PubMed ID: 18990985
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 3p partial trisomy and 13q partial monosomy with congenital malformations and psychomotor developmental delay.
    Rodovalho-Doriqui MJ; Freitas PL; Pinho JD; Cavalli LR; Pereira SR
    Genet Mol Res; 2013 Jul; 12(3):2562-6. PubMed ID: 23979887
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A trisomy 13 case with Robertsonian translocation presenting with atypical findings.
    Demirel G; Oguz SS; Celik IH; Sandal G; Uras N; Erdeve O; Dilmen U
    Genet Couns; 2010; 21(3):293-7. PubMed ID: 20964120
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Partial trisomy of chromosome 13--diagnosis confirmed with the FISH in situ hybridization technique].
    Obersztyn E; Stankiewicz P; Bocian E; Stańczak H; Mazurczak T
    Pediatr Pol; 1996 Mar; 71(3):247-52. PubMed ID: 8966097
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
    de Ravel T; Aerssens P; Vermeesch JR; Fryns JP
    Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Holoprosencephaly-polydactyly (pseudotrisomy 13) syndrome: case report and diagnostic criteria.
    Sergi C; Gekas J; Kamnasaran D
    Fetal Pediatr Pathol; 2012 Oct; 31(5):315-8. PubMed ID: 22432933
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4.
    Battaglia A; Brothman AR; Carey JC
    Am J Med Genet; 2002 Sep; 112(1):103-6. PubMed ID: 12239731
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Further delineation of pseudotrisomy 13 syndrome: a case without polydactyly.
    Ramos-Arroyo MA; de Miguel C; Valiente A; Moreno-Laguna S
    Am J Med Genet; 1994 Apr; 50(2):177-9. PubMed ID: 8010349
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Trisomy 9p: a clinical picture and the importance of examining the family].
    van Ravenswaaij-Arts C; van der Looij E; Smeets D
    Ned Tijdschr Geneeskd; 1999 Mar; 143(13):682-6. PubMed ID: 10321302
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Smith-Lemli-Opitz syndrome in trisomy 13: how does the mix work?
    Alkuraya FS; Picker J; Irons MB; Kimonis VE
    Birth Defects Res A Clin Mol Teratol; 2005 Aug; 73(8):569-71. PubMed ID: 15965973
    [TBL] [Abstract][Full Text] [Related]  

  • 14. "Holoprosencephaly-polydactyly" (pseudotrisomy 13) syndrome: expansion of the phenotypic spectrum.
    Lurie IW; Wulfsberg EA
    Am J Med Genet; 1993 Sep; 47(3):405-9. PubMed ID: 8135289
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Dental management of an adolescent with trisomy 13 syndrome: a case report.
    Klein U; Buehler BA
    J Dent Child (Chic); 2004; 71(1):91-5. PubMed ID: 15272666
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Partial 6q monosomy/partial 12q trisomy in a child with features of Kabuki make-up syndrome.
    Jardine PE; Burvill-Holmes LC; Schutt WH; Lunt PW
    Clin Dysmorphol; 1993 Jul; 2(3):269-73. PubMed ID: 8287190
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pure partial trisomy 4q syndrome in a child with der(9)ins(9;4)(q34.3;q26q35.2)mat.
    Topcu V; Ilgin-Ruhi H; Yurur-Kutlay N; Ekici C; Vicdan A; Tukun FA
    Genet Couns; 2014; 25(1):1-6. PubMed ID: 24783648
    [TBL] [Abstract][Full Text] [Related]  

  • 18. FISH diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly (C) phenotype.
    Chu TW; Teebi AS; Gibson L; Breg WR; Yang-Feng TL
    Am J Med Genet; 1994 Aug; 52(1):92-6. PubMed ID: 7977471
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
    El-Ruby M; Hemly NA; Zaki MS
    Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Patau syndrome with long survival in a case of unusual mosaic trisomy 13.
    Fogu G; Maserati E; Cambosu F; Moro MA; Poddie F; Soro G; Bandiera P; Serra G; Tusacciu G; Sanna G; Mazzarello V; Montella A
    Eur J Med Genet; 2008; 51(4):303-14. PubMed ID: 18495567
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.