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 *

124 related articles for article (PubMed ID: 6984625)

  • 1. [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]  

  • 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. 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]  

  • 4. Trisomy 4p in a family with A t(4;15).
    Hustinx WJ; Gabreëls JM; Kirkels VG; Korten JJ; Scheres JM; Joosten EM; Rutten FJ
    Ann Genet; 1975 Mar; 18(1):13-9. PubMed ID: 1080034
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [Unbalanced translocation 8/X in a girl].
    Ickstadt A; Palitzsch D; Foerster W; Fuhrmann-Rieger A
    Monatsschr Kinderheilkd; 1989 Apr; 137(4):239-42. PubMed ID: 2733701
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Asymmetric clinical and cytogenetic findings in a 4-year-old girl with trisomy 18 mosaicism.
    Rao KW; Buchanan PD; Aylsworth AS
    Birth Defects Orig Artic Ser; 1978; 14(6C):349-54. PubMed ID: 728589
    [No Abstract]   [Full Text] [Related]  

  • 8. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
    Peeters H; Vermeesch J; Fryns JP
    Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Trisomy 18 mosaicism in a mildly retarded boy with postnatal overgrowth.
    Plessis G; Le Treust M; Lemaire F; Maugard T; Cau D
    Ann Genet; 1997; 40(4):235-7. PubMed ID: 9526621
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?
    van Buggenhout G; Decock P; Fryns JP
    Genet Couns; 1996; 7(1):53-9. PubMed ID: 8652089
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
    Chen H; Tuck-Muller CM; Batista DA; Wertelecki W
    Am J Med Genet; 1995 Mar; 56(2):219-33. PubMed ID: 7625449
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Isochromosome-formation in chromosome 9.
    Miller K; Arslan-Kirchner M
    Ann Genet; 1994; 37(2):78-81. PubMed ID: 7985983
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
    Lukusa T; van den Berghe L; Smeets E; Fryns JP
    Ann Genet; 1999; 42(4):215-20. PubMed ID: 10674161
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype.
    D'Amato Sizonenko L; Ng D; Oei P; Winship I
    Am J Med Genet; 2002 Jul; 111(1):19-26. PubMed ID: 12124728
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Trisomy 20q caused by der(4) t(4;20) (q35;q13.1): report of a new patient and review of the literature.
    Plotner PL; Smith JL; Northrup H
    Am J Med Genet; 2002 Jul; 111(1):71-5. PubMed ID: 12124739
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 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. [A new chromosome syndrome: trisomy 8 mosaicism].
    Kosztolányi G; Bühler EM; Stalder GR
    Orv Hetil; 1977 Oct; 118(43):2593-6. PubMed ID: 917541
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.