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Journal Abstract Search

290 related items for PubMed ID: 3067576

  • 1. 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; 31(3):553-7. PubMed ID: 3067576
    [Abstract] [Full Text] [Related]

  • 2. 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]

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

  • 4. Ectrodactyly and proximal/intermediate interstitial deletion 7q.
    McElveen C, Carvajal MV, Moscatello D, Towner J, Lacassie Y.
    Am J Med Genet; 1995 Mar 13; 56(1):1-5. PubMed ID: 7747769
    [Abstract] [Full Text] [Related]

  • 5. Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3.
    Pfeiffer RA, Legat G, Trautmann U.
    Ann Genet; 1992 Mar 13; 35(1):41-6. PubMed ID: 1610119
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation.
    Mdzin R, Ko C, Abdul Latif Z, Zakaria Z.
    Singapore Med J; 2008 Nov 17; 49(11):e336-9. PubMed ID: 19037546
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: case report and review.
    Boles RG, Pober BR, Gibson LH, Willis CR, McGrath J, Roberts DJ, Yang-Feng TL.
    Am J Med Genet; 1995 Jan 16; 55(2):155-60. PubMed ID: 7717414
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].
    Wilson MG, Towner JW, Forsman I, Siris E.
    Am J Med Genet; 1979 Jan 16; 3(2):155-74. PubMed ID: 474629
    [Abstract] [Full Text] [Related]

  • 12. Interstitial deletion of the band 4p15.3 defined by sequential replication banding.
    Davies J, Voullaire L, Bankier A.
    Ann Genet; 1990 Jan 16; 33(2):92-5. PubMed ID: 2241091
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. 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 01; 37(4):471-4. PubMed ID: 2260590
    [Abstract] [Full Text] [Related]

  • 15. The 4q-Syndrome.
    Strehle EM, Ahmed OA, Hameed M, Russell A.
    Genet Couns; 2001 Dec 01; 12(4):327-39. PubMed ID: 11837601
    [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. 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 02; 24(3):393-414. PubMed ID: 2425619
    [Abstract] [Full Text] [Related]

  • 19. Interstitial deletion of the short arm of chromosome 1 (46XY, del(1)(p13p22.3)).
    Mattia FR, Wardinsky TD, Tuttle DJ, Grix A, Smith KA, Walling P.
    Am J Med Genet; 1992 Nov 15; 44(5):551-4. PubMed ID: 1481806
    [Abstract] [Full Text] [Related]

  • 20. [Killian-Teschler-Nicola syndrome (Pallister-Killian syndrome, mosaic tetrasomy 12p)].
    Pankau R, Diebold U, Jenderny J, Kautza M, Dörner K.
    Monatsschr Kinderheilkd; 1992 Jun 15; 140(6):340-2. PubMed ID: 1640944
    [No Abstract] [Full Text] [Related]

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