BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

338 related articles for article (PubMed ID: 6686175)

  • 1. [Rare case of mosaicism for chromosome 18, karyotype: 46, XX, del(18) (p11)/46, XX, i(18q)].
    Badalian LO; Mutovin GR; Malygina NA; Petrukhin AS
    Genetika; 1983 Nov; 19(11):1912-5. PubMed ID: 6686175
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Mosaic variant of the translocation form of syndrome 18q-].
    Badalian LO; Dement'eva GM; Malygina NA; Mutovin GR; Petrukhin AS
    Genetika; 1981; 17(10):1867-71. PubMed ID: 7198075
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.
    Fryns JP; Kleczkowska A; Jaeken J; Van Herck K; Van den Berghe MH
    Ann Genet; 1989; 32(3):177-9. PubMed ID: 2486064
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Two cases of 18q- syndrome with mosaicism (46,XX / 46,XX, 18q-)].
    Lejeune J; Berger R; Réthoré MO; Lafourcade J; Dutrillaux B; Canlorbe P; Labrune B
    Ann Genet; 1967 Mar; 10(1):18-24. PubMed ID: 5300122
    [No Abstract]   [Full Text] [Related]  

  • 5. [Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18].
    Vivarelli R; Paolieri M; Anichini C; Scarinci R; Berardi R; Rosaia L; Pucci L
    Boll Soc Ital Biol Sper; 1992 Apr; 68(4):263-9. PubMed ID: 1463601
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A patient with hypopituitarism and isochromosome 18q mosaicism.
    Turan S; Saka N; Guney I; Bereket A
    Horm Res; 2005; 64(6):261-5. PubMed ID: 16272819
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Tetrasomy of the short arm of human chromosome 18: cytogenetics and phenotypic disorders].
    Kuleshov NP; Zaletaev DV; Levina LIa; Dement'eva GM; Arbuzov SP
    Tsitol Genet; 1985; 19(6):452-6. PubMed ID: 4089954
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chromosome 18 aneuploidy: anatomical variations observed in cases of full and mosaic trisomy 18 and a case of deletion of the short arm of chromosome 18.
    Urban B; Bersu ET
    Am J Med Genet; 1987 Jun; 27(2):425-34. PubMed ID: 3605225
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Skin pigment anomalies and mosaicism for a double autosomal trisomy (48,XX,+18,+20).
    Devriendt K; Matthijs G; Meireleire J; Roelen L; van Buggenhout G; Fryns JP
    Genet Couns; 1998; 9(4):283-6. PubMed ID: 9894166
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism.
    Habecker-Green JG; Naeem R; Gold H; O'Grady JP; Kanaan C; Bayer-Zwirello L; Murray MS; Cohn GM
    J Perinatol; 1998; 18(5):395-8. PubMed ID: 9766419
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome.
    Urioste M; Visedo G; Sanchís A; Sentís C; Villa A; Ludeña P; Hortigüela JL; Martínez-Frías ML; Fernández-Piqueras J
    Am J Med Genet; 1994 Jan; 49(1):77-82. PubMed ID: 8172255
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal detection of monosomy 18p and trisomy 18q mosaicism with unexpected fetal phenotype.
    Sutton SD; Ridler MA
    J Med Genet; 1986 Jun; 23(3):258-9. PubMed ID: 3723556
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case of mosaic trisomy 14 due to an isochromosome, i(14q).
    Ozawa N; Xu ZD; Soh K; Takabayashi T; Sato S; Yajima A; Suzuki M; Ikeuchi T; Tonomura A
    Jinrui Idengaku Zasshi; 1984 Mar; 29(1):69-76. PubMed ID: 6748330
    [No Abstract]   [Full Text] [Related]  

  • 14. 18q- and 18q+ mosaicism in a mentally retarded boy.
    Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF
    Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotype-karyotype correlations in dup(18q): report of a case and review.
    Razavi-Encha F; Raoul O; Lescs MC; Danan C
    Am J Med Genet; 1985 Jul; 21(3):591-5. PubMed ID: 4025391
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Non-mosaic trisomy 16 in a third-trimester fetus.
    Yancey MK; Hardin EL; Pacheco C; Kuslich CD; Donlon TA
    Obstet Gynecol; 1996 May; 87(5 Pt 2):856-60. PubMed ID: 8677115
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Isochromosome 18p in a mother and her child.
    Abeliovich D; Dagan J; Levy A; Steinberg A; Zlotogora J
    Am J Med Genet; 1993 Jun; 46(4):392-3. PubMed ID: 8357009
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Three cell line mosaicism involving structural and numerical abnormalities of chromosome 18 in a 3.5-year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XX.
    Sutcliffe MJ; Mueller OT; Kousseff BG; Dumont DP; McFarland JA; Mawani F; Conforto D; Ranells JD
    Am J Med Genet; 2001 Aug; 102(2):192-9. PubMed ID: 11477615
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Developmental and other pathologic changes in syndromes caused by chromosome abnormalities.
    Gilbert EF; Opitz JM
    Perspect Pediatr Pathol; 1982; 7():1-63. PubMed ID: 6214761
    [No Abstract]   [Full Text] [Related]  

  • 20. [Chromosomal mosaicism in the r (15) syndrome].
    Malygina NA; Mutovin GR; Filina NP; Akif'ev AP
    Genetika; 1980; 16(11):2029-33. PubMed ID: 7193157
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.