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Journal Abstract Search

411 related items for PubMed ID: 8839888

  • 1. Further delineation of 7p trisomy. Case report and review of literature.
    Pallotta R, Dalprà L, Fusilli P, Zuffardi O.
    Ann Genet; 1996; 39(3):152-8. PubMed ID: 8839888
    [Abstract] [Full Text] [Related]

  • 2. Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype.
    Fryns JP, Kleczkowska A, Kenis H, Decock P, Van den Berghe H.
    Ann Genet; 1989; 32(3):174-6. PubMed ID: 2573314
    [Abstract] [Full Text] [Related]

  • 3. Partial trisomy 15q: report of a patient and literature review.
    Chandler K, Schrander-Stumpel CT, Engelen J, Theunissen P, Fryns JP.
    Genet Couns; 1997; 8(2):91-7. PubMed ID: 9219006
    [Abstract] [Full Text] [Related]

  • 4. Emerging phenotype of duplication (7p): a report of three cases and review of the literature.
    Milunsky JM, Wyandt HE, Milunsky A.
    Am J Med Genet; 1989 Jul; 33(3):364-8. PubMed ID: 2679090
    [Abstract] [Full Text] [Related]

  • 5. [Trisomy 5p: a report of 2 cases].
    Alvarez-Coca J, García-Alix A, Delicado A, González M, Escribá R, López Pajares I, Morena V, Peralta A.
    An Esp Pediatr; 1985 Mar 31; 22(4):288-92. PubMed ID: 4003955
    [Abstract] [Full Text] [Related]

  • 6. Duplication of 7p21.2-->pter due to maternal 7p;21q translocation: implications for critical segment assignment in the 7p duplication syndrome.
    Cai T, Yu P, Tagle DA, Xia J.
    Am J Med Genet; 1999 Oct 08; 86(4):305-11. PubMed ID: 10494083
    [Abstract] [Full Text] [Related]

  • 7. Duplication 7p de novo and literature review.
    Zerres K, Schwanitz G, Gellissen K, Schroers L, Sohler R.
    Ann Genet; 1989 Oct 08; 32(4):225-9. PubMed ID: 2692511
    [Abstract] [Full Text] [Related]

  • 8. Secondary trisomy or mosaic "tetrasomy" 8p.
    Robinow M, Haney N, Chen H, Sorauf T, Van Dyke DL, Babu VR, Powell S, Maliszewski W, Guerin S, Landers JW.
    Am J Med Genet; 1989 Mar 08; 32(3):320-4. PubMed ID: 2729351
    [Abstract] [Full Text] [Related]

  • 9. Partial 3p trisomy and different rearrangements involving chromosome 3 in the proposita's family.
    de Pina Neto JM, Ferrari I.
    Am J Med Genet; 1980 Mar 08; 5(1):25-33. PubMed ID: 7395898
    [Abstract] [Full Text] [Related]

  • 10. Duplication 3p syndrome: report of a new case and review of the literature.
    Charrow J, Cohen MM, Meeker D.
    Am J Med Genet; 1981 Mar 08; 8(4):431-6. PubMed ID: 7246613
    [Abstract] [Full Text] [Related]

  • 11. [Trisomy 10q24--10qter].
    Dutrillaux B, Laurent C, Bernasconi S, Lejeune J.
    Ann Genet; 1975 Dec 08; 18(4):217-22. PubMed ID: 1083188
    [Abstract] [Full Text] [Related]

  • 12. 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 Dec 08; 7(1):61-5. PubMed ID: 8652090
    [Abstract] [Full Text] [Related]

  • 13. De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome?
    Redha MA, Krishna Murthy DS, al-Awadi SA, al-Sulaiman IS, Sabry MA, el-Bahey SA, Farag TI.
    Ann Genet; 1996 Dec 08; 39(1):5-9. PubMed ID: 9297445
    [Abstract] [Full Text] [Related]

  • 14. Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature.
    Brisset S, Joly G, Ozilou C, Lapierre JM, Gosset P, LeLorc'h M, Raoul O, Turleau C, Vekemans M, Romana SP.
    Am J Med Genet; 2002 Dec 15; 113(4):339-45. PubMed ID: 12457405
    [Abstract] [Full Text] [Related]

  • 15. [A new case of trisomy 5p].
    Antonenko VG, Levina LIa, Chudnova VI.
    Genetika; 1985 Dec 15; 21(12):2066-70. PubMed ID: 4085794
    [Abstract] [Full Text] [Related]

  • 16. ["De novo" partial trisomy 16p (author's transl)].
    Gabarrón Llamas J, Cabrerizo Portero D, Montserrat Bernal F, Rodríguez Costa T, Cabrerizo Merino C, Rodríguez López F.
    An Esp Pediatr; 1981 Dec 15; 15(6):587-91. PubMed ID: 7337311
    [Abstract] [Full Text] [Related]

  • 17. Trisomy 7p: report of 2 patients and literature review.
    Arens YH, Toutain A, Engelen JJ, Offermans JP, Hamers AJ, Schrander JJ, Pulles-Heintzberger CF, Schrander-Stumpel CT.
    Genet Couns; 2000 Dec 15; 11(4):347-54. PubMed ID: 11140412
    [Abstract] [Full Text] [Related]

  • 18. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
    Liang DS, Wu LQ, Cai F, Xia K, Long ZG, Pan Q, Dai HP, Xia JH.
    Yi Chuan Xue Bao; 2005 Feb 15; 32(2):124-9. PubMed ID: 15759858
    [Abstract] [Full Text] [Related]

  • 19. Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature.
    Taysi K, Chao WT, Monaghan N, Monaco MP.
    Ann Genet; 1983 Feb 15; 26(4):243-6. PubMed ID: 6364954
    [Abstract] [Full Text] [Related]

  • 20. 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 Feb 15; 32(3):177-9. PubMed ID: 2486064
    [Abstract] [Full Text] [Related]

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