BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

261 related articles for article (PubMed ID: 3565467)

  • 1. Trisomy 14 mosaicism syndrome.
    Lipson MH
    Am J Med Genet; 1987 Mar; 26(3):541-4. PubMed ID: 3565467
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Trisomy 9 mosaicism in a girl with multiple malformations.
    Diaz-Mares L; Molina B; Carnevale A
    Ann Genet; 1990; 33(3):165-8. PubMed ID: 2288462
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. [Hereditary mosaicism: normal-trisomy D, chromosome fragility and new type of mosaicism with D ringformation in descendents].
    Zdansky R; Rett A; Piperger A
    Fortschr Med; 1972 Jul; 90(19):748-52. PubMed ID: 5073851
    [No Abstract]   [Full Text] [Related]  

  • 6. Diploid-triploid mosaicism: delineation of the syndrome.
    Tharapel AT; Wilroy RS; Martens PR; Holbert JM; Summitt RL
    Ann Genet; 1983; 26(4):229-33. PubMed ID: 6607703
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Trisomy 14 Mosaicism: a case without evidence of neurodevelopmental delay and a review of the literature.
    Merritt TA; Natarajan G
    Am J Perinatol; 2007 Oct; 24(9):563-6. PubMed ID: 17893842
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 46,XY-47,XY,C+ mosaicism in a male infant with multiple anomalies.
    Oikawa K; Kajii T; Shimba H; Sasaki M
    Ann Genet; 1969 Jun; 12(2):102-6. PubMed ID: 5308379
    [No Abstract]   [Full Text] [Related]  

  • 9. Unusual mosaic trisomy 13 through 13/13 translocation and monosomy 13 with a small ring.
    Jalal SM; Martin JA; Benjamin TR; Kukolich MK; Townsend-Parcham JK
    Ann Genet; 1990; 33(3):173-5. PubMed ID: 2288463
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Brief clinical report: non-mosaic partial tetrasomy and partial trisomy 9.
    Shapiro SD; Hansen KL; Littlefield CA
    Am J Med Genet; 1985 Feb; 20(2):271-6. PubMed ID: 3976720
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development.
    Ausems MG; Van Spijker HG; Dijkhuis HJ; Swanenburg De Veye HF; Bijlsma JB
    Genet Couns; 1996; 7(1):61-5. PubMed ID: 8652090
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Syndrome of multiple abnormalities in a child with mosaicism 46, XY/47, XY, +E].
    Balcar-Boroń A; Sawa H; Slowik J; Marcinkowska A; Robińska E
    Pediatr Pol; 1977 Oct; 52(10):1161-4. PubMed ID: 583678
    [No Abstract]   [Full Text] [Related]  

  • 15. Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p.
    De Pater JM; Van Tintelen JP; Stigter R; Brouwers HA; Scheres JM
    Genet Couns; 2000; 11(3):241-7. PubMed ID: 11043432
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A case of neonatal Pallister-Killian syndrome (tetrasomy 12p)].
    González de Dios J; García-Alix Pérez A; Díaz de Bustamante A; Delicado Navarro A; Arés Segura S; Salas Hernández S; Quero Jiménez J
    An Esp Pediatr; 1993 Mar; 38(3):277-9. PubMed ID: 8460851
    [No Abstract]   [Full Text] [Related]  

  • 17. [9p trisomy syndrome. Two new cases (author's transl)].
    Martín Sánchez A; Delicado A; Izquierdo M; Oliver A; López Pajares I; Gracia R; Peralta A
    An Esp Pediatr; 1981 May; 14(5):344-51. PubMed ID: 7294523
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A de novo tandem duplication 15(q21 leads to qter) mosaic.
    Yip MY; Parsons A; Hultén M
    Clin Genet; 1982 Jul; 22(1):1-6. PubMed ID: 7172470
    [No Abstract]   [Full Text] [Related]  

  • 19. Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy.
    Schinzel A; Kotzot D; Brecevic L; Robinson WP; Dutly F; Dauwerse H; Binkert F; Baumer A; Ausserer B
    Eur J Hum Genet; 1997; 5(5):308-14. PubMed ID: 9412788
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The characteristic phenotype of distal 9q3 trisomy is due to duplication of band 9q32.
    Kleczkowska A; Fryns JP; Lemay P; Van den Berghe H
    Genet Couns; 1993; 4(3):217-21. PubMed ID: 8267931
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.