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 *

120 related articles for article (PubMed ID: 2459386)

  • 1. Deletion of band 5q21 in association with a de novo translocation involving 2p and 5q.
    Yung JF; Williamson N; Salafsky I; Hoo JJ
    J Med Genet; 1988 Aug; 25(8):570-2. PubMed ID: 2459386
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Concurrent de novo interstitial deletion of band 2p22 and reciprocal translocation (3;7)(p21;q22).
    Webb GC; Keith CG; Campbell NT
    J Med Genet; 1988 Feb; 25(2):125-7. PubMed ID: 3346886
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Double chromosome anomaly: interstitial deletion 5q and reciprocal translocation (1;11)(p22;q21).
    de Michelena MI; Villacorta J; Chávez J
    Am J Med Genet; 1990 May; 36(1):29-32. PubMed ID: 2185634
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A de novo 6p interstitial deletion and a complex translocation involving chromosomes 2, 6, and 14 in a mildly developmentally delayed patient.
    Misceo D; Bjørgo K; Ormerod E; Ringen Ø; Rocchi M; van der Hagen CB; Frengen E
    Am J Med Genet A; 2008 Dec; 146A(24):3230-3. PubMed ID: 19012337
    [No Abstract]   [Full Text] [Related]  

  • 5. Developmental delay and dysmorphic features associated with a previously undescribed deletion on chromosome 1.
    Barton JS; O'Loughlin J; Howell RT; L'e Orme R
    J Med Genet; 1995 Aug; 32(8):636-7. PubMed ID: 7473657
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A de novo interstitial deletion of chromosome 15 band q25 as revealed by FISH-technique.
    Verma RS; Kleyman SM; Giridharan R; Ramesh KH
    Clin Genet; 1996 Jun; 49(6):303-5. PubMed ID: 8884079
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Partial monosomy 21 (q11.2→q21.3) combined with 3p25.3→pter monosomy due to an unbalanced translocation in a patient presenting dysmorphic features and developmental delay.
    dos Santos AP; Vieira TP; Simioni M; Monteiro FP; Gil-da-Silva-Lopes VL
    Gene; 2013 Jan; 513(2):301-4. PubMed ID: 23031812
    [TBL] [Abstract][Full Text] [Related]  

  • 9. De novo translocation (2;18)(q21;q22) in a child with severe epilepsy, developmental delay and mild dysmorphism.
    Bal M; Schrander-Stumpel CT; Meers LE; Theunissen PM; Hamers AJ; Wennekes MJ; Engelen JJ
    Genet Couns; 2000; 11(3):221-7. PubMed ID: 11043430
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Incidental finding of paternal UPD15 in a child with a deletion of 11q21-q22.3, presenting with developmental delay, coloboma and characteristic dysmorphic features.
    Tucker T; Steinraths M; Oh T; Nelson TN; Van Allen MI; Brown L; Schlade-Bartusiak K
    Clin Dysmorphol; 2016 Apr; 25(2):77-81. PubMed ID: 26636500
    [No Abstract]   [Full Text] [Related]  

  • 11. De novo 10q22 interstitial deletion.
    Cook L; Weaver DD; Hartsfield JK; Vance GH
    J Med Genet; 1999 Jan; 36(1):71-2. PubMed ID: 9950372
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A case of ring chromosome 2 with growth retardation, mild dysmorphism, and microdeletion of 2p detected using FISH.
    Dee SL; Clark AT; Willatt LR; Yates JR
    J Med Genet; 2001 Sep; 38(9):E32. PubMed ID: 11546833
    [No Abstract]   [Full Text] [Related]  

  • 13. Molecular cytogenetic characterization of 2p23.2p23.3 deletion in a child with developmental delay, hypotonia and cryptorchism.
    Rocca MS; Faletra F; Devescovi R; Gasparini P; Pecile V
    Eur J Med Genet; 2013 Jan; 56(1):62-5. PubMed ID: 23142270
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deletion of 5q by t(5;17) in therapy-related myelodysplastic syndrome.
    Vandenberghe EA; Mecucci C; Delannoy A; Van den Berghe H
    Cancer Genet Cytogenet; 1990 Aug; 48(1):49-52. PubMed ID: 2372787
    [No Abstract]   [Full Text] [Related]  

  • 15. Translocation 5;21 and interstitial deletion of chromosome 7 in a case of chronic myelomonocytic leukemia.
    Sherrington PD; Nacheva E; Fischer P; Rees JK; Hoyle C; Dyer M; Harper P; Knight C; Hayhoe FG
    Cancer Genet Cytogenet; 1988 Apr; 31(2):247-52. PubMed ID: 3162398
    [TBL] [Abstract][Full Text] [Related]  

  • 16. De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma.
    Calzolari E; Palazzi P; Aiello V; Mazzeo E; Perri P; Minelli A; del Senno L; Patracchini P; Bernardi F
    Hum Genet; 1987 Sep; 77(1):51-4. PubMed ID: 3502696
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An unbalanced translocation between chromosomes 2p and 6p associated with Axenfeld-Rieger anomaly type 3, hearing loss, developmental delay, and distinct facial dysmorphism.
    Li F; Batista DA; Maumenee I; Wang T
    Am J Med Genet A; 2010 May; 152A(5):1318-21. PubMed ID: 20425844
    [No Abstract]   [Full Text] [Related]  

  • 18. Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.
    Fernandez T; Morgan T; Davis N; Klin A; Morris A; Farhi A; Lifton RP; State MW
    Am J Hum Genet; 2004 Jun; 74(6):1286-93. PubMed ID: 15106122
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Double translocation 46, XX, t(2; 5), t(2; 18) with major reproduction problems].
    Sidaner I; Nivelon-Chevallier A; Mugneret F; Turc-Carel C
    J Genet Hum; 1988 Jan; 36(1-2):89-92. PubMed ID: 3379383
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A complex chromosome translocation resulting in deletion 11p and associated with uveal colobomata.
    Friling R; Yassur Y; Abeliovich D; Biedner B; Galil A; Dagan J; Carmi R
    Ophthalmic Genet; 1995 Jun; 16(2):71-4. PubMed ID: 7493159
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.