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Journal Abstract Search

148 related items for PubMed ID: 7262872

  • 1. Trisomy 18q. A case report and review of karyotype-phenotype correlations.
    Matsuoka R, Matsuyama S, Yamamoto Y, Kuroki Y, Matsui I.
    Hum Genet; 1981; 57(1):78-82. PubMed ID: 7262872
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Partial trisomy 16q21➔qter due to an unbalanced segregation of a maternally inherited balanced translocation 46,XX,t(15;16)(p13;q21): a case report and review of literature.
    Mishra R, Paththinige CS, Sirisena ND, Nanayakkara S, Kariyawasam UGIU, Dissanayake VHW.
    BMC Pediatr; 2018 Jan 08; 18(1):4. PubMed ID: 29310616
    [Abstract] [Full Text] [Related]

  • 4. Congenital polyvalvular disease in trisomy 18: echocardiographic diagnosis.
    Balderston SM, Shaffer EM, Washington RL, Sondheimer HM.
    Pediatr Cardiol; 1990 Jul 08; 11(3):138-42. PubMed ID: 2395741
    [Abstract] [Full Text] [Related]

  • 5. Partial trisomy 18 in a family with a translocation (18;21)(q21;q22).
    Niazi M, Coleman DV, Saldaña-Garcia P.
    J Med Genet; 1978 Apr 08; 15(2):148-51. PubMed ID: 641950
    [Abstract] [Full Text] [Related]

  • 6. Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.
    Cetin Z, Mihci E, Keser I, Karaali K, Berker S, Luleci G.
    Genet Couns; 2012 Apr 08; 23(2):239-47. PubMed ID: 22876583
    [Abstract] [Full Text] [Related]

  • 7. Trisomy 8p by malsegregation of a t(5;8)(p15;p11)mat in a case of XY pure gonadal dysgenesis.
    Memo L, Lenzini E, Baccichetti C.
    Ann Genet; 1988 Apr 08; 31(3):181-5. PubMed ID: 3066281
    [Abstract] [Full Text] [Related]

  • 8. A female with XO/XY mosaicism and partial trisomy 9p.
    Klasen M, Hansmann I, Schmid M, Schmidtke J.
    J Med Genet; 1981 Dec 08; 18(6):482. PubMed ID: 7334513
    [No Abstract] [Full Text] [Related]

  • 9. Trisomy 18q: 46,XX,-10,+der(10) t(10;18) (p15;q12) pat: a case report.
    Murthy SK, Kar B, Prabhakara K, Krishnamurthy DS.
    Ann Genet; 1992 Dec 08; 35(3):174-7. PubMed ID: 1466569
    [Abstract] [Full Text] [Related]

  • 10. Partial trisomy 18(q11 leads to qter) in an infant and aborted fetus resulting from a balanced paternal translocation t(13;18)(q32:q11).
    Rosenmann A, Isacson M, Cohen R, Segal M, Cohen MM.
    Ann Genet; 1978 Mar 08; 21(1):60-4. PubMed ID: 308346
    [Abstract] [Full Text] [Related]

  • 11. Trisomy 18 and 18p- features in a case of isochromosome 18q [46,XY,i(18q)]: prenatal diagnosis and autopsy report.
    Wurster-Hill DH, Marin-Padilla JM, Moeschler JB, Park JP, McDermet M.
    Clin Genet; 1991 Feb 08; 39(2):142-8. PubMed ID: 2015695
    [Abstract] [Full Text] [Related]

  • 12. Partial trisomy 8 (trisomy 8q2106 leads to 8qter).
    Abuelo D, Perl DP, Henkle C, Richardson A.
    J Med Genet; 1977 Dec 08; 14(6):463-6. PubMed ID: 604499
    [Abstract] [Full Text] [Related]

  • 13. A 14-year follow-up of a case detected prenatally of partial trisomy 13q21.32-qter and monosomy 18q22.3-qter as a result of a maternal complex chromosome rearrangement involving chromosomes 6, 13, and 18.
    Quadrelli R, Quadrelli A, Milunsky A, Zou YS, Huang XL, Viera E, Mechoso B, Bellini S, Costabel M, Vaglio A.
    Genet Test Mol Biomarkers; 2009 Jun 08; 13(3):387-93. PubMed ID: 19473082
    [Abstract] [Full Text] [Related]

  • 14. Congenital heart anomalies in the trisomy 18 syndrome, with reference to congenital polyvalvular disease.
    Matsuoka R, Misugi K, Goto A, Gilbert EF, Ando M.
    Am J Med Genet; 1983 Apr 08; 14(4):657-68. PubMed ID: 6846400
    [Abstract] [Full Text] [Related]

  • 15. Karyotype/phenotype correlation in partial trisomies of the long arm of chromosome 16: case report and review of literature.
    Laus AC, Baratela WA, Laureano LA, Santos SA, Huber J, Ramos ES, Rebelo CC, Squire JA, Martelli L.
    Am J Med Genet A; 2012 Apr 08; 158A(4):821-7. PubMed ID: 22354628
    [Abstract] [Full Text] [Related]

  • 16. Partial trisomy 6q, due to balanced maternal translocation (6;22) (q21; p13) or (q21; pter).
    Stamberg J, Shapiro J, Valle D, Kuhajda FP, Thomas G, Wissow L.
    Clin Genet; 1981 Feb 08; 19(2):122-5. PubMed ID: 7471508
    [Abstract] [Full Text] [Related]

  • 17. 47,XX,+der(18),t(9;18)(p24;q21) mat: a distinct partial trisomy 18q--syndrome?
    Bass HN, Weber-Parisi F, Sparkes RS.
    J Med Genet; 1978 Oct 08; 15(5):391-5. PubMed ID: 739531
    [Abstract] [Full Text] [Related]

  • 18. Partial trisomy 12p. A newborn child with karyotype 46,XY,der(11), t(11; 12) (q25; p11) mat. Case report and review.
    Ottolina de Bracamonte N, Velazco JQ, Hammond Figueroa FG.
    Acta Cient Venez; 1982 Oct 08; 33(4):342-7. PubMed ID: 7186725
    [No Abstract] [Full Text] [Related]

  • 19. Two cases with partial trisomy 9: cytogenetic and clinical findings.
    Ozer O, Derbent M, Sahin FI, Yilmaz Z.
    Genet Couns; 2010 Oct 08; 21(2):205-13. PubMed ID: 20681221
    [Abstract] [Full Text] [Related]

  • 20. [Partial trisomy 14q II.--Partial trisomy 14q due to a maternal t(12; 14) (q24.4; q21)].
    Turleau C, Grouchy J, Bocquentin F, Roubin M, Colin FC.
    Ann Genet; 1975 Mar 08; 18(1):41-4. PubMed ID: 1080037
    [Abstract] [Full Text] [Related]

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