BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

231 related articles for article (PubMed ID: 6638063)

  • 1. Trisomy 18/trisomy 13 mosaicism in an adult with profound mental retardation and multiple malformations.
    Wilson WG; Shires MA; Willson KA; Wyandt HE; Harris LM; Kelly TE
    Am J Med Genet; 1983 Sep; 16(1):131-6. PubMed ID: 6638063
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Trisomy 14 mosaicism: case report and review.
    Johnson VP; Aceto T; Likness C
    Am J Med Genet; 1979; 3(4):331-9. PubMed ID: 474633
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A mildly retarded woman with 46,XX/47,XX, + 18 mosaicism.
    Bensen JT; Steele MW
    Am J Med Genet; 1985 Oct; 22(2):343-6. PubMed ID: 4050867
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)].
    Turleau C; Rethoré MO; Junien C; Lejeune J; de Grouchy J
    Ann Genet; 1979; 22(3):178-81. PubMed ID: 316677
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Long survival in trisomy-13-syndrome: 21 cases including prolonged survival in two patients 11 and 19 years old.
    Redheendran R; Neu RL; Bannerman RM
    Am J Med Genet; 1981; 8(2):167-72. PubMed ID: 7282771
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Trisomy 14 mosaicism with t(14;15)(q11;p11) in offspring of a balanced translocation carrier mother.
    Fujimoto A; Lin MS; Korula SR; Wilson MG
    Am J Med Genet; 1985 Oct; 22(2):333-42. PubMed ID: 4050866
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant.
    Milunsky JM; Wyandt HE; Huang XL; Kang XZ; Elias ER; Milunsky A
    Am J Med Genet; 1996 Jan; 61(3):269-73. PubMed ID: 8741873
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Trisomy 8: an international study of 70 patients.
    Riccardi VM
    Birth Defects Orig Artic Ser; 1977; 13(3C):171-84. PubMed ID: 890109
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Natural history of mosaic trisomy 14 syndrome.
    Fujimoto A; Allanson J; Crowe CA; Lipson MH; Johnson VP
    Am J Med Genet; 1992 Sep; 44(2):189-96. PubMed ID: 1456290
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Unilateral microtia in an infant with trisomy 18 mosaicism.
    Giannatou E; Leze H; Katana A; Kolialexi A; Mavrou A; Kanavakis E; Kitsiou-Tzeli S
    Genet Couns; 2009; 20(2):181-7. PubMed ID: 19650416
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Trisomy 14 mosaicism in a liveborn male: clinical report and review of the literature.
    Kaplan LC; Wayne A; Crowell S; Latt SA
    Am J Med Genet; 1986 Apr; 23(4):925-30. PubMed ID: 3515939
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Trisomy 7p due to a mosaic normal/dir dup(7)(p13----p22). Syndrome delineation, critical segment assignment, and a comment on duplications.
    CantĂș JM; Rivas F; Ruiz C; Barajas LO; Moller M; Rivera H
    Ann Genet; 1985; 28(4):254-7. PubMed ID: 3879442
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).
    Gentile M; Buonadonna AL; Cariola F; Fiorente P; Valenzano MC; Guanti G
    J Med Genet; 1999 Jan; 36(1):77-82. PubMed ID: 9950374
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Monosomy/trisomy 4q12 to q13 mosaicism in a retarded and dysmorphic girl].
    Pescia G; Tonella A; Jotterand-Bellomo M
    Ann Genet; 1982; 25(2):110-2. PubMed ID: 6984625
    [No Abstract]   [Full Text] [Related]  

  • 17. Trisomy 8 mosaicism: a further five cases illustrating marked clinical and cytogenetic variability.
    Jordan MA; Marques I; Rosendorff J; de Ravel TJ
    Genet Couns; 1998; 9(2):139-46. PubMed ID: 9664211
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Constitutional partial 1q trisomy mosaicism and Wilms tumor.
    Mark HF; Wyandt H; Pan A; Milunsky JM
    Cancer Genet Cytogenet; 2005 Oct; 162(2):166-71. PubMed ID: 16213366
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Optic atrophy, microcephaly, mental retardation and mosaic variegated aneuploidy: a human mitotic mutation.
    Bitoun P; Martin-Pont B; Tamboise E; Gaudelus J
    Ann Genet; 1994; 37(2):75-7. PubMed ID: 7985982
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Duplication 12q mosaicism in two unrelated patients with a similar syndrome.
    Harrod MJ; Byrne JB; Dev VG; Francke U
    Am J Med Genet; 1980; 7(2):123-9. PubMed ID: 7468644
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.