BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 14738116)

  • 1. Paracentric inversion in the short arm of chromosome 1. Report of a family and review of the literature.
    Cogulu O; Ozkinay F; Gunduz C; Cankaya T; Ozkinay C
    Genet Couns; 2003; 14(4):419-23. PubMed ID: 14738116
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial paracentric inversion of 1p.
    Romain DR; Columbano-Green LM; Whyte S; Smythe RH; Parfitt RG; Gebbie OB; Chapman CJ
    Am J Med Genet; 1983 Apr; 14(4):629-34. PubMed ID: 6846398
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial paracentric inversion of the short arm of chromosome 3.
    Fryns JP; van den Berghe H
    Ann Genet; 1979; 22(3):163-4. PubMed ID: 316673
    [TBL] [Abstract][Full Text] [Related]  

  • 4. De novo paracentric inversion in a microcephalic boy: 46,XY, inv(14)(q13q24).
    Jaeken J; Fryns JP; Standaert L; De Cock P; Van den Berghe H
    Ann Genet; 1980; 23(2):105-7. PubMed ID: 6967281
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Paracentric inversion X(q21.2q24) associated with mental retardation in males and normal ovarian function in females.
    Abeliovich D; Dagan J; Kimchi-Sarfaty C; Zlotogora J
    Am J Med Genet; 1995 Jan; 55(3):359-62. PubMed ID: 7726237
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial pericentric and paracentric inversions of chromosome 1.
    Johnson DD; Dobyns WB; Gordon H; Dewald GW
    Hum Genet; 1988 Aug; 79(4):315-20. PubMed ID: 3410456
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Three large Danish families with a paracentric inversion in the short arm of chromosome N. 5.
    Baggesen K; Friedrich U; Jensen PK; Rasmussen K
    Ann Genet; 1988; 31(1):50-2. PubMed ID: 3258494
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypes.
    Estop AM; Bansal V; Lin A; Levinson F; Karlin SM; Surti U; Wenger SL; Steele MW
    Am J Med Genet; 1994 Feb; 49(4):410-3. PubMed ID: 8160735
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A familial paracentric inv(1)(q42q44) resulting in a child with a del(1)(q42) karyotype.
    Speevak M; Hunter AG; Hughes H; Cox DM
    Ann Genet; 1985; 28(3):177-80. PubMed ID: 3879153
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial pericentric inversion of chromosome 13, 46,XX,inv (13)(p13;q11): a new variant.
    Mohammed FM; Krishna Murthy DS; Farag TI; al-Awadi SA; al-Othman SA; Hammad I
    Ann Genet; 1993; 36(3):181-5. PubMed ID: 8117067
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal detection of de novo paracentric inversion 46, XX inv (14) (q22q32.1) in a normal child: report and review of the literature.
    Hales HA; Peterson CM; Carey J; Hecht BK; Hecht F
    Am J Med Genet; 1993 Nov; 47(6):848-51. PubMed ID: 8279482
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Recombinant chromosome 9 possibly derived from breakage and reunion of sister chromatids within a paracentric inversion loop.
    Phelan MC; Stevenson RE; Anderson EV
    Am J Med Genet; 1993 May; 46(3):304-8. PubMed ID: 8488876
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
    Piovani G; Borsani G; Bertini V; Kalscheuer VM; Viertel P; Bellotti D; Valseriati D; Barlati S
    Eur J Med Genet; 2006; 49(3):215-23. PubMed ID: 16762823
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Reproductive risk of paracentric inversion carriers: report of two unrelated cases with paracentric inversion of the long arm of chromosome 3.
    Kasai R; Narahara K; Kikkawa K; Takahashi Y; Wakita Y; Kimura S; Kataoka N; Kimoto H
    Jinrui Idengaku Zasshi; 1985 Jun; 30(2):57-67. PubMed ID: 3841372
    [No Abstract]   [Full Text] [Related]  

  • 15. Cytogenetic study of a family with an aberrant inv ((15p+ q-) chromosome inherited through five generations.
    Podugol'nikova OA; Batienko GS
    Sov Genet; 1974 May; 8(4):518-25. PubMed ID: 4412695
    [No Abstract]   [Full Text] [Related]  

  • 16. Paracentric inversion of chromosome 14 plus rare 9p variant in a couple with habitual spontaneous abortion.
    Turczynowicz S; Sharma P; Smith A; Davidson AA
    Ann Genet; 1992; 35(1):58-60. PubMed ID: 1610123
    [TBL] [Abstract][Full Text] [Related]  

  • 17. U-type exchange in a paracentric inversion as a possible mechanism of origin of an inverted tandem duplication of chromosome 8.
    Mitchell JJ; Vekemans M; Luscombe S; Hayden M; Weber B; Richter A; Sparkes R; Kojis T; Watters G; Der Kaloustian VM
    Am J Med Genet; 1994 Feb; 49(4):384-7. PubMed ID: 8160729
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Correlation of clinical phenotype with a pericentric inversion of chromosome 9 and genetic counseling.
    Demirhan O; Pazarbasi A; Suleymanova-Karahan D; Tanriverdi N; Kilinc Y
    Saudi Med J; 2008 Jul; 29(7):946-51. PubMed ID: 18626518
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mental retardation and Y/8 translocation [karyotype: 46,XY, t(Y;8)(q12;q24)] in father and son.
    Fryns JP; Kleczkowska A; Dereymaeker AM; Van den Berghe H
    Helv Paediatr Acta; 1988 Aug; 43(1-2):87-90. PubMed ID: 3170249
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Pericentric inversion of chromosome 9. Summary of the authors' results].
    Vargas de los Monteros MT; Fernández-Novoa García MC; Salas Herrero E; San Martín Díez MV; Novales Huertas MA
    An Esp Pediatr; 1990 Nov; 33(5):442-9. PubMed ID: 2096758
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.