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160 related items for PubMed ID: 9863609

  • 1. De novo unbalanced translocation resulting in monosomy for proximal 14q and distal 4p in a fetus with intrauterine growth retardation, Wolf-Hirschhorn syndrome, hypertrophic cardiomyopathy, and partial hemihypoplasia.
    Chen CP, Chern SR, Lee CC, Chen WL, Chen MH, Chang KM.
    J Med Genet; 1998 Dec; 35(12):1050-3. PubMed ID: 9863609
    [Abstract] [Full Text] [Related]

  • 2. De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1 → pter) and 14q (14q32.31 → qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction, and single umbilical artery: prenatal diagnosis and molecular cytogenetic characterization.
    Chen CP, Fu CH, Chern SR, Wu PS, Su JW, Lee CC, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2013 Sep; 52(3):401-6. PubMed ID: 24075381
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  • 6. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
    Zhu CJ, Huang ZY, Wu WQ, Zhao Q, Jiang HY, Xie JS.
    Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
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  • 7. Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome.
    Estabrooks LL, Lamb AN, Aylsworth AS, Callanan NP, Rao KW.
    J Med Genet; 1994 Feb; 31(2):103-7. PubMed ID: 8182713
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  • 8. Clinical, cytogenetic and molecular investigation in a fetus with Wolf-Hirschhorn syndrome with paternally derived 4p deletion. Case report and review of the literature.
    Dietze I, Fritz B, Huhle D, Simoens W, Piecha E, Rehder H.
    Fetal Diagn Ther; 2004 Feb; 19(3):251-60. PubMed ID: 15067236
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  • 9. Prenatal diagnosis and fetal pathology of partial trisomy 20P-monosomy 4P resulting from paternal translocation.
    Vamos E, Pratola D, Van Regemorter N, Freund M, Flament-Durand J, Rodesch F.
    Prenat Diagn; 1985 Feb; 5(3):209-14. PubMed ID: 2410900
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  • 10. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication.
    Chen CP, Lin CJ, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Chen LF, Yang CW, Wang W.
    Taiwan J Obstet Gynecol; 2016 Aug; 55(4):596-601. PubMed ID: 27590390
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  • 11. The Wolf-Hirschhorn syndrome in fetuses.
    Tachdjian G, Fondacci C, Tapia S, Huten Y, Blot P, Nessmann C.
    Clin Genet; 1992 Dec; 42(6):281-7. PubMed ID: 1493641
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  • 12. Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p.
    McGhee EM, Qu Y, Wohlferd MM, Goldberg JD, Norton ME, Cotter PD.
    Clin Genet; 2001 Apr; 59(4):274-8. PubMed ID: 11298684
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  • 13. Prenatal diagnosis of a fetus with unbalanced translocation (4;13)(p16;q32) with overlapping features of Patau and Wolf-Hirschhorn syndromes.
    Tapper JK, Zhang S, Harirah HM, Panova NI, Merryman LS, Hawkins JC, Lockhart LH, Gei AB, Velagaleti GV.
    Fetal Diagn Ther; 2002 Apr; 17(6):347-51. PubMed ID: 12393964
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  • 14. Prenatal diagnosis and molecular cytogenetics in a case of partial trisomy 14 and monosomy 21.
    Lee C, Fowler DJ, Lemyre E, Sandstrom MM, Holmes LB, Morton CC.
    Am J Med Genet; 2001 May 01; 100(3):246-50. PubMed ID: 11343311
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  • 15. Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.
    Chen CP, Su YN, Chen YY, Su JW, Chern SR, Chen YT, Chen WL, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2011 Dec 01; 50(4):506-11. PubMed ID: 22212326
    [Abstract] [Full Text] [Related]

  • 16. Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21)(p16.3;q22.1): relevance to the Wolf-Hirschhorn and Down syndrome critical regions.
    Sebastio G, Perone L, Guzzetta V, Sebastio L, Vicari L, Della Casa R, Gurrieri F, Zappata S, Pomponi MG, Mazzei A, Neri G, Andria G, Brahe C.
    Am J Med Genet; 1996 May 17; 63(2):366-72. PubMed ID: 8725787
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  • 17. Two sibs with Wolf-Hirschhorn and DiGeorge deletions resulting from an unbalanced chromosome rearrangement, 45,XX/XY, der(4)t(4;22) (p16.3;q11.2) mat,-22.
    Reddy KS, Sulcova V, Siassi B.
    J Med Genet; 1996 Oct 17; 33(10):852-5. PubMed ID: 8933340
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  • 18. Prenatal detection of congenital hypospadias in the Wolf-Hirschhorn (4p-) syndrome.
    Viñals F, Sepulveda W, Selman E.
    Prenat Diagn; 1994 Dec 17; 14(12):1166-9. PubMed ID: 7899285
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  • 19. Microarray analysis of unbalanced translocation in Wolf-Hirschhorn syndrome.
    Dai Y, Yang J, Chen Y, Bao L, Cheng Q.
    Pediatr Int; 2013 Jun 17; 55(3):368-70. PubMed ID: 23782367
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  • 20. Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals: clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndrome.
    Wheeler PG, Weaver DD, Palmer CG.
    Am J Med Genet; 1995 Feb 13; 55(4):462-5. PubMed ID: 7762587
    [Abstract] [Full Text] [Related]

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