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 *

125 related articles for article (PubMed ID: 16276093)

  • 1. Trisomy of chromosome 18 in the baboon (Papio hamadryas anubis).
    Howell KH; Hubbard GB; Moore CM; Dunn BG; von Kap-Herr C; Raveendran M; Rogers JA; Leland MM; Brasky KM; Nathanielsz PW; Schlabritz-Loutsevitch NE
    Cytogenet Genome Res; 2006; 112(1-2):76-81. PubMed ID: 16276093
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Trisomy 17 in a baboon (Papio hamadryas) with polydactyly, patent foramen ovale and pyelectasis.
    Moore CM; Hubbard GB; Dick E; Dunn BG; Raveendran M; Rogers J; Williams V; Gomez JJ; Butler SD; Leland MM; Schlabritz-Loutsevitch NE
    Am J Primatol; 2007 Oct; 69(10):1105-18. PubMed ID: 17330307
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Teratoma with trisomy 16 in a baboon (Papio hamadryas).
    Moore CM; McKeand J; Witte SM; Hubbard GB; Rogers J; Leland MM
    Am J Primatol; 1998; 46(4):323-32. PubMed ID: 9839905
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype.
    Mewar R; Harrison W; Weaver DD; Palmer C; Davee MA; Overhauser J
    Am J Med Genet; 1994 Aug; 52(2):178-83. PubMed ID: 7802005
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. Trisomy 16 in a pigtailed macaque (M. nemestrina) with multiple anomalies and developmental delays.
    Ruppenthal GC; Moore CM; Best RG; Walker-Gelatt CG; Delio PJ; Sackett GP
    Am J Ment Retard; 2004 Jan; 109(1):9-20. PubMed ID: 14651446
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy.
    Schinzel A; Kotzot D; Brecevic L; Robinson WP; Dutly F; Dauwerse H; Binkert F; Baumer A; Ausserer B
    Eur J Hum Genet; 1997; 5(5):308-14. PubMed ID: 9412788
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial trisomy 14q due to maternal t(4;14)(p16;q32) in a dysmorphic newborn.
    Dundar M; Uzak A; Saatci C; Akalin H
    Genet Couns; 2011; 22(3):287-92. PubMed ID: 22029170
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].
    Ulmer R; Pfeiffer RA; Kollert A; Beinder E
    Z Geburtshilfe Neonatol; 2000; 204(1):1-7. PubMed ID: 10721179
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism in a patient with linear and whorled nevoid hypermelanosis.
    Hartmann A; Hofmann UB; Hoehn H; Broecker EB; Hamm H
    Pediatr Dermatol; 2004; 21(6):636-41. PubMed ID: 15575846
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Iniencephaly and chromosome mosaicism: a report of two cases.
    Halder A; Agarwal S; Pandey A
    Congenit Anom (Kyoto); 2005 Sep; 45(3):102-5. PubMed ID: 16131369
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cytogenetic abnormalities in orthopedic patients.
    Cowell HR; Clark CE
    Clin Orthop Relat Res; 1978 Sep; (135):4-14. PubMed ID: 152176
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Trisomy 9 mosaicism in a girl with multiple malformations.
    Diaz-Mares L; Molina B; Carnevale A
    Ann Genet; 1990; 33(3):165-8. PubMed ID: 2288462
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Overgrowth and trisomy 15q26.1-qter including the IGF1 receptor gene: report of two families and review of the literature.
    Faivre L; Gosset P; Cormier-Daire V; Odent S; Amiel J; Giurgea I; Nassogne MC; Pasquier L; Munnich A; Romana S; Prieur M; Vekemans M; De Blois MC; Turleau C
    Eur J Hum Genet; 2002 Nov; 10(11):699-706. PubMed ID: 12404101
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding.
    Polityko A; Starke H; Rumyantseva N; Claussen U; Liehr T; Raskin S
    Cytogenet Genome Res; 2005; 111(2):171-4. PubMed ID: 16103660
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Trisomy 22 confirmed by fluorescent in situ hybridization.
    Stratton RF; DuPont BR; Mattern VL; Young RS; McCourt JW; Moore CM
    Am J Med Genet; 1993 Apr; 46(1):109-12. PubMed ID: 8494030
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.