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 *

153 related articles for article (PubMed ID: 7460380)

  • 21. Trisomy 13 in a 4-year-old child.
    Fernández-Novoa C; Hevia A; Martínez JJ; San Martín V; Galera H
    Hum Genet; 1980; 53(3):297-8. PubMed ID: 7372331
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies.
    Uwineza A; Hitayezu J; Jamar M; Caberg JH; Murorunkwere S; Janvier N; Bours V; Mutesa L
    J Trop Pediatr; 2016 Feb; 62(1):38-45. PubMed ID: 26507407
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Partial trisomy of chromosome 18 (pter leads to q11): a discussion on the identification of the critical segment.
    San Martin V; Fernandez-Novoa C; Hevia A; Novales A; Fornell J; Galera H
    Ann Genet; 1981; 24(4):248-50. PubMed ID: 6977308
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Small metacentric nonsatellited extra chromosome: report of five mentally retarded individuals and review of literature. Contribution to further delineation of a new syndrome.
    Nielsen KB; Dyggve H; Friedrich U; Hobolth N; Lyngbye T; Mikkelsen M
    Hum Genet; 1978 Oct; 44(1):59-69. PubMed ID: 711239
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Monosomy, trisomy, fragile sites, and rearrangements of chromosome no. 1 in a mentally retarded male with multiple congenital anomalies.
    Neu RL; Kousseff BG; Madan S; Essig YP; Miller K; Tedesco TA
    Clin Genet; 1988 Feb; 33(2):73-7. PubMed ID: 3359669
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Interstitial deletion of chromosome 13: prognosis and adult phenotype.
    Dean JC; Simpson S; Couzin DA; Stephen GS
    J Med Genet; 1991 Aug; 28(8):533-5. PubMed ID: 1920369
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Characterization of a de novo partial trisomy 22q13-qter in a patient by microFISH.
    Petek E; Köstl G; Mutz I; Wagner K; Kroisel PM
    Clin Dysmorphol; 2000 Jan; 9(1):55-7. PubMed ID: 10649799
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Trisomy 17p due to a t(8;17) (p23;p11.2)pat translocation. Case report and review of the literature.
    Schrander-Stumpel C; Schrander J; Fryns JP; Hamers G
    Clin Genet; 1990 Feb; 37(2):148-52. PubMed ID: 2178819
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Partial trisomy for short arm of chromosome 5.
    Yasutomo K; Suzue T; Nishioka A; Kozan H; Sekiguchi T; Ohara K; Okamoto T; Iwai T; Endo S
    Acta Paediatr Jpn; 1993 Aug; 35(4):336-9. PubMed ID: 8379327
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Complete and partial trisomy of different segments of chromosome 8: case reports and review.
    Fineman RM; Ablow RC; Breg WR; Wing SD; Rose JS; Rothman SL; Warpinski J
    Clin Genet; 1979 Dec; 16(6):390-8. PubMed ID: 527246
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Delineation of a characteristic phenotype in distal trisomy 2q.
    Kyllerman M; Wahlström J; Westerberg B; Gustavson KH
    Helv Paediatr Acta; 1984 Dec; 39(5-6):499-508. PubMed ID: 6543860
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Kleeblattschädel anomaly and partial trisomy for chromosome 13 (47,XY,+der(13),t(3,13)(q24; q14).
    McCorquodale M; Erickson RP; Robinson M; Roszczipka K
    Clin Genet; 1980 Jun; 17(6):409-14. PubMed ID: 7398112
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations].
    Bocian E; Nowakowska B; Obersztyn E; Borg K; Chudoba I; Kostyk E; Kruczek A; Pietrzyk J; Mazurczak T
    Med Wieku Rozwoj; 2006; 10(1 Pt 2):211-25. PubMed ID: 17028390
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Trisomy 6qter.
    Turleau C; de Grouchy J
    Clin Genet; 1981 Mar; 19(3):202-6. PubMed ID: 7273465
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Phenotypic and cytogenetic spectrum of 9p trisomy.
    Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
    Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
    [TBL] [Abstract][Full Text] [Related]  

  • 36. An extra small metacentric chromosome in association with multiple congenital abnormalities.
    Finley WH; Finley SC; Monsky D
    J Med Genet; 1971 Sep; 8(3):381-3. PubMed ID: 5097148
    [No Abstract]   [Full Text] [Related]  

  • 37. Cytogenetics in mentally defective children with anomalies: a controlled study.
    Summitt RL
    J Pediatr; 1969 Jan; 74(1):58-66. PubMed ID: 5782825
    [No Abstract]   [Full Text] [Related]  

  • 38. 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]  

  • 39. Trisomy 16p in a liveborn infant and review of trisomy 16p.
    O'Connor TA; Higgins RR
    Am J Med Genet; 1992 Feb; 42(3):316-9. PubMed ID: 1536169
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Partial trisomy 20 confirmed by gene dosage studies.
    Rudd NL; Bain HW; Giblett E; Chen SH; Worton RG
    Am J Med Genet; 1979; 4(4):357-64. PubMed ID: 231907
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.