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 *

77 related articles for article (PubMed ID: 2610489)

  • 21. Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridization.
    Zenger-Hain JL; Van Dyke DL; Wiktor A; Walker H; Feldman GL
    Am J Med Genet; 1993 Dec; 47(8):1198-201. PubMed ID: 8291556
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Partial duplication of 4q12q13 leads to a mild phenotype.
    Shashi V; Berry MN; Santos C; Pettenati MJ
    Am J Med Genet; 1999 Sep; 86(1):51-3. PubMed ID: 10440828
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A new case of dup(1)(q21.2q12) in an individual with mild mental retardation.
    Faas BH; Mieloo H; Van Es-Van Gaal JW; Van Ravenswaaij C
    Genet Couns; 2003; 14(4):407-11. PubMed ID: 14738114
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prominent satellites in oligophrenic, malformed patients: incidence, frequency of satellite associations and karyotype-phenotype comparisons.
    Varella-Garcia M; Tajara EH
    Acta Anthropogenet; 1982; 6(1):69-84. PubMed ID: 7138650
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Wolf syndrome. Apropos of 2 cases].
    García González P; Pedraz García C; Merino Marcos L; Salazar Veloz J; Escudero Bueno G; Salazar Villalobos V
    An Esp Pediatr; 1983 Feb; 18(2):113-7. PubMed ID: 6881733
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular cytogenetic characterization of a small, familial supernumerary ring chromosome 7 associated with mental retardation and an abnormal phenotype.
    Tan-Sindhunata G; Castedo S; Leegte B; Mulder I; vd Veen AY; vd Hout AH; Wiersma TJ; van Essen AJ
    Am J Med Genet; 2000 May; 92(2):147-52. PubMed ID: 10797441
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cytogenetic studies in patients with multiple anomalies with or without mental retardation.
    Berry R; Smith AC; McGavran L; O'Hanlon K
    Birth Defects Orig Artic Ser; 1987; 23(6):100-10. PubMed ID: 3435749
    [No Abstract]   [Full Text] [Related]  

  • 28. [Clinical case of tandem translocation between chromosomes 13 and 15].
    Badalian LO; Arkhipov BA; Malygina NA; Patrukhin AS; Lysov VL
    Tsitol Genet; 1985; 19(4):304-8. PubMed ID: 4049521
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Cytogenetic study for a child patient with mental retardation and eye multiple malformation].
    Qin M
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1997 Aug; 19(4):309-11. PubMed ID: 10453574
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mosaic isochromosome 8p.
    Tilstra DJ; Grove M; Spencer AC; Norwood TH; Pagon RA
    Am J Med Genet; 1993 Jun; 46(5):517-9. PubMed ID: 8322812
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Complex chromosome rearrangement in a retarded girl with malformations.
    Kitsiou S; Tsezou A; Bartsocas CS; Tapratzi P; Kourakis G; Papas C; Dellagrammaticas H
    Ann Genet; 1987; 30(1):59-61. PubMed ID: 3498433
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Deletion of 2p: a cytogenetic and clinical update.
    Neidich J; Zackai E; Aronson M; Emanuel BS
    Am J Med Genet; 1987 Jul; 27(3):707-10. PubMed ID: 3477100
    [TBL] [Abstract][Full Text] [Related]  

  • 33. De novo complex chromosome rearrangement: a study of two patients.
    Melo DG; Huber J; Giuliani LR; Mazzucatto LF; Riegel M; Pina-Neto JM
    Genet Couns; 2004; 15(3):303-10. PubMed ID: 15517822
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Inversion 8 and consecutive trisomy of region 8q22----qter].
    Andrle M; Erlach A; Schweizer C
    Wien Klin Wochenschr; 1987 Sep; 99(18):638-41. PubMed ID: 3687023
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
    Esmer MC; Carnevale A; Gómez L; del Castillo V; Frías S
    Rev Invest Clin; 1996; 48(1):27-33. PubMed ID: 8815483
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Probable position of MN gene locus on the human karyotype].
    Dinić B; Stojimirović E; Garzicić B; Ajdarić
    Bilt Hematol Transfuz; 1975; 3(1-2):57-62. PubMed ID: 1225320
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Meiotic consequences of pericentric inversions of chromosome 13.
    Wenger SL; Steele MW
    Am J Med Genet; 1981; 9(4):275-83. PubMed ID: 7294066
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Deletions of proximal 15q without Prader-Willi syndrome.
    Greenberg F; Ledbetter DH
    Am J Med Genet; 1987 Dec; 28(4):813-20. PubMed ID: 3688019
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
    Batista DA; Pai GS; Stetten G
    Am J Med Genet; 1994 Nov; 53(3):255-63. PubMed ID: 7856662
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Coexistence of inverted Y, chromosome 15p+ and abnormal phenotype.
    Acar H; Cora T; Erkul I
    Genet Couns; 1999; 10(2):163-70. PubMed ID: 10422010
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.