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Journal Abstract Search

388 related items for PubMed ID: 3067575

  • 1. Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.
    Lin AE, Garver KL, Diggans G, Clemens M, Wenger SL, Steele MW, Jones MC, Israel J.
    Am J Med Genet; 1988 Nov; 31(3):533-48. PubMed ID: 3067575
    [Abstract] [Full Text] [Related]

  • 2. Deletions of different segments of the long arm of chromosome 4.
    Mitchell JA, Packman S, Loughman WD, Fineman RM, Zackai E, Patil SR, Emanual B, Bartley JA, Hanson JW.
    Am J Med Genet; 1981 Nov; 8(1):73-89. PubMed ID: 7246608
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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 17; 31(3):553-7. PubMed ID: 3067576
    [Abstract] [Full Text] [Related]

  • 5. Interstitial deletions 4q21.1q25 and 4q25q27: phenotypic variability and relation to Rieger anomaly.
    Kulharya AS, Maberry M, Kukolich MK, Day DW, Schneider NR, Wilson GN, Tonk V.
    Am J Med Genet; 1995 Jan 16; 55(2):165-70. PubMed ID: 7717415
    [Abstract] [Full Text] [Related]

  • 6. Terminal and interstitial deletions of the long arm of chromosome 7: a review with five new cases.
    Young RS, Weaver DD, Kukolich MK, Heerema NA, Palmer CG, Kawira EL, Bender HA.
    Am J Med Genet; 1984 Feb 16; 17(2):437-50. PubMed ID: 6199974
    [Abstract] [Full Text] [Related]

  • 7. 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 16; 37(4):471-4. PubMed ID: 2260590
    [Abstract] [Full Text] [Related]

  • 8. Deletions of the long arm of chromosome 6: two new cases and review of the literature.
    Young RS, Fidone GS, Reider-Garcia PA, Hansen KL, McCombs JL, Moore CM.
    Am J Med Genet; 1985 Jan 16; 20(1):21-9. PubMed ID: 3881954
    [Abstract] [Full Text] [Related]

  • 9. 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 16; 24(3):421-32. PubMed ID: 3728561
    [Abstract] [Full Text] [Related]

  • 10. Interstitial deletion of long arm of chromosome 13.
    Carnevale A, Frias S, Alcantar R.
    Ann Genet; 1984 Jul 16; 27(1):49-52. PubMed ID: 6609673
    [Abstract] [Full Text] [Related]

  • 11. Terminal deletion of chromosome 10q26: delineation of two clinical phenotypes.
    Petit P, Devriendt K, Azou M, Gewillig M, Fryns JP.
    Genet Couns; 1998 Jul 16; 9(4):271-5. PubMed ID: 9894164
    [Abstract] [Full Text] [Related]

  • 12. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
    Battaglia A, Hoyme HE, Dallapiccola B, Zackai E, Hudgins L, McDonald-McGinn D, Bahi-Buisson N, Romano C, Williams CA, Brailey LL, Zuberi SM, Carey JC.
    Pediatrics; 2008 Feb 16; 121(2):404-10. PubMed ID: 18245432
    [Abstract] [Full Text] [Related]

  • 13. Interstitial deletion of (17)(p11.2p11.2) in nine patients.
    Smith AC, McGavran L, Robinson J, Waldstein G, Macfarlane J, Zonona J, Reiss J, Lahr M, Allen L, Magenis E.
    Am J Med Genet; 1986 Jul 16; 24(3):393-414. PubMed ID: 2425619
    [Abstract] [Full Text] [Related]

  • 14. Child with velocardiofacial syndrome and del (4)(q34.2): another critical region associated with a velocardiofacial syndrome-like phenotype.
    Tsai CH, Van Dyke DL, Feldman GL.
    Am J Med Genet; 1999 Feb 12; 82(4):336-9. PubMed ID: 10051168
    [Abstract] [Full Text] [Related]

  • 15. A specific syndrome due to deletion of the distal long arm of chromosome 1.
    Meinecke P, Vögtel D.
    Am J Med Genet; 1987 Oct 12; 28(2):371-6. PubMed ID: 3322005
    [Abstract] [Full Text] [Related]

  • 16. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.
    Sukumar S, Wang S, Hoang K, Vanchiere CM, England K, Fick R, Pagon B, Reddy KS.
    Am J Med Genet; 1999 Nov 05; 87(1):17-22. PubMed ID: 10528241
    [Abstract] [Full Text] [Related]

  • 17. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3).
    Copelli S, del Rey G, Heinrich J, Coco R.
    Am J Med Genet; 1995 Jan 02; 55(1):77-9. PubMed ID: 7702102
    [Abstract] [Full Text] [Related]

  • 18. 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 02; 8(7):519-26. PubMed ID: 10909852
    [Abstract] [Full Text] [Related]

  • 19. Terminal deletion of the long arm of chromosome 4. Report of a case of 46, XY, del(4)(q31) and review of 4q- syndrome.
    Yu CW, Chen H, Baucum RW, Hand AM.
    Ann Genet; 1981 Jul 02; 24(3):158-61. PubMed ID: 6974525
    [Abstract] [Full Text] [Related]

  • 20. Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patients.
    Obregon MG, Mingarelli R, Digilio MC, Zelante L, Giannotti A, Sabatino G, Dallapiccola B.
    Ann Genet; 1992 Jul 02; 35(4):208-12. PubMed ID: 1296516
    [Abstract] [Full Text] [Related]

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