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359 related items for PubMed ID: 7717413

  • 1. Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literature.
    Chitayat D, Ruvalcaba RH, Babul R, Teshima IE, Posnick JC, Vekemans MJ, Scarpelli H, Thuline H.
    Am J Med Genet; 1995 Jan 16; 55(2):147-54. PubMed ID: 7717413
    [Abstract] [Full Text] [Related]

  • 2. Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardation.
    White DM, Pillers DA, Reiss JA, Brown MG, Magenis RE.
    Am J Med Genet; 1995 Jul 17; 57(4):588-97. PubMed ID: 7573135
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletion.
    Wieczorek D, Krause M, Majewski F, Albrecht B, Horn D, Riess O, Gillessen-Kaesbach G.
    Eur J Hum Genet; 2000 Jul 13; 8(7):519-26. PubMed ID: 10909852
    [Abstract] [Full Text] [Related]

  • 5. 7p deletion syndrome: an adult with mild manifestations.
    Grebe TA, Stevens MA, Byrne-Essif K, Cassidy SB.
    Am J Med Genet; 1992 Sep 01; 44(1):18-23. PubMed ID: 1519644
    [Abstract] [Full Text] [Related]

  • 6. Proximal interstitial 6q deletion: a recognizable syndrome.
    Kumar R, Riordan D, Dawson AJ, Chudley AE.
    Am J Med Genet; 1997 Aug 22; 71(3):353-6. PubMed ID: 9268108
    [Abstract] [Full Text] [Related]

  • 7. A specific syndrome due to deletion of the distal long arm of chromosome 1.
    Meinecke P, Vögtel D.
    Am J Med Genet; 1987 Oct 22; 28(2):371-6. PubMed ID: 3322005
    [Abstract] [Full Text] [Related]

  • 8. Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature.
    de Die-Smulders CE, Engelen JJ, Schrander-Stumpel CT, Govaerts LC, de Vries B, Vles JS, Wagemans A, Schijns-Fleuren S, Gillessen-Kaesbach G, Fryns JP.
    Am J Med Genet; 1995 Nov 20; 59(3):369-74. PubMed ID: 8599364
    [Abstract] [Full Text] [Related]

  • 9. Interstitial deletion of 17p11.2: case report and review.
    Hamill MA, Roberts SH, Maguire MJ, Laurence KM.
    Ann Genet; 1988 Nov 20; 31(1):36-8. PubMed ID: 3281568
    [Abstract] [Full Text] [Related]

  • 10. [Wolf syndrome. Apropos of 2 cases].
    García González P, Pedraz García C, Merino Marcos L, Salazar Veloz J, Escudero Bueno G, Salazar Villalobos V.
    An Esp Pediatr; 1983 Feb 20; 18(2):113-7. PubMed ID: 6881733
    [Abstract] [Full Text] [Related]

  • 11. High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome.
    Fang YY, Bain S, Haan EA, Eyre HJ, MacDonald M, Wright TJ, Altherr MR, Riess O, Sutherland G, Callen DF.
    Am J Med Genet; 1997 Sep 05; 71(4):453-7. PubMed ID: 9286454
    [Abstract] [Full Text] [Related]

  • 12. Interstitial 6q duplication in an adult male without growth delay or severe mental retardation.
    Cappon SL, Duncan AM, Khalifa MM.
    Med Sci Monit; 2000 Sep 05; 6(3):581-5. PubMed ID: 11208374
    [Abstract] [Full Text] [Related]

  • 13. A child with multiple congenital anomalies and karyotype 46,XY,del(14)(q31q32.3): further delineation of chromosome 14 interstitial deletion syndrome.
    Gorski JL, Uhlmann WR, Glover TW.
    Am J Med Genet; 1990 Dec 05; 37(4):471-4. PubMed ID: 2260590
    [Abstract] [Full Text] [Related]

  • 14. A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4.
    Beall MH, Falk RE, Ying KL.
    Am J Med Genet; 1988 Nov 05; 31(3):553-7. PubMed ID: 3067576
    [Abstract] [Full Text] [Related]

  • 15. Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.
    Stratton RF, Dobyns WB, Greenberg F, DeSana JB, Moore C, Fidone G, Runge GH, Feldman P, Sekhon GS, Pauli RM.
    Am J Med Genet; 1986 Jul 05; 24(3):421-32. PubMed ID: 3728561
    [Abstract] [Full Text] [Related]

  • 16. Mild phenotype due to inverse duplication 4p16.3 - P15.3 including the Wolf-Hirschhorn critical region.
    Tschernigg M, Petek E, Wagner K, Kroisel PM.
    Genet Couns; 2002 Jul 05; 13(1):29-33. PubMed ID: 12017235
    [Abstract] [Full Text] [Related]

  • 17. Interstitial deletion of the band 4p15.3 defined by sequential replication banding.
    Davies J, Voullaire L, Bankier A.
    Ann Genet; 1990 Jul 05; 33(2):92-5. PubMed ID: 2241091
    [Abstract] [Full Text] [Related]

  • 18. Interstitial deletion of the short arm of chromosome 4. A phenotype distinct from the Wolf-Hirschhorn syndrome.
    Fryns JP, Yang-Aisheng, Kleczkowska A, Lemmens F, Vandecasseye W, van den Berghe H.
    Ann Genet; 1989 Jul 05; 32(1):59-61. PubMed ID: 2751251
    [Abstract] [Full Text] [Related]

  • 19. Cytogenetic abnormalities in two new patients with Pitt-Rogers-Danks phenotype.
    Lindeman-Kusse MC, Van Haeringen A, Hoorweg-Nijman JJ, Brunner HG.
    Am J Med Genet; 1996 Dec 02; 66(1):104-12. PubMed ID: 8957526
    [Abstract] [Full Text] [Related]

  • 20. Interstitial deletion of 4p15.32p16.3 in a boy with minor anomalies, hearing loss, borderline intelligence, and oligodontia.
    Kozma C, Chong SS, Meck JM.
    Am J Med Genet; 1999 Oct 08; 86(4):316-20. PubMed ID: 10494085
    [Abstract] [Full Text] [Related]

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