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Journal Abstract Search

314 related items for PubMed ID: 11837601

  • 1. The 4q-Syndrome.
    Strehle EM, Ahmed OA, Hameed M, Russell A.
    Genet Couns; 2001; 12(4):327-39. PubMed ID: 11837601
    [Abstract] [Full Text] [Related]

  • 2. 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; 49(11):e336-9. PubMed ID: 19037546
    [Abstract] [Full Text] [Related]

  • 3. The spectrum of 4q- syndrome illustrated by a case series.
    Strehle EM, Gruszfeld D, Schenk D, Mehta SG, Simonic I, Huang T.
    Gene; 2012 Sep 15; 506(2):387-91. PubMed ID: 22771923
    [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 15; 31(3):553-7. PubMed ID: 3067576
    [Abstract] [Full Text] [Related]

  • 5. Additional patient with del(12)(q21.2q22): further evidence for a candidate region for cardio-facio-cutaneous syndrome?
    Rauen KA, Albertson DG, Pinkel D, Cotter PD.
    Am J Med Genet; 2002 Jun 01; 110(1):51-6. PubMed ID: 12116271
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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 16; 31(3):533-48. PubMed ID: 3067575
    [Abstract] [Full Text] [Related]

  • 8. Smith-Magenis syndrome and tetralogy of Fallot.
    Sweeney E, Peart I, Tofeig M, Kerr B.
    J Med Genet; 1999 Jun 16; 36(6):501-2. PubMed ID: 10874646
    [No Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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 Dec 16; 8(1):73-89. PubMed ID: 7246608
    [Abstract] [Full Text] [Related]

  • 11. Multigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27-q28.1 microdeletion.
    Hickey SE, Biswas S, Thrush DL, Pyatt RE, Gastier-Foster JM, Astbury C, Atkin J.
    Eur J Med Genet; 2013 Sep 16; 56(9):521-5. PubMed ID: 23895773
    [Abstract] [Full Text] [Related]

  • 12. Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q.
    Cousineau AJ, Higgins JV, Scott-Emuakpor AB, Mody G.
    Am J Med Genet; 1983 Jan 16; 14(1):29-35. PubMed ID: 6829609
    [Abstract] [Full Text] [Related]

  • 13. Familial deletion of 22q11.2.
    Rodríguez Criado G, Gruesomontero J, Delicado Navarro A.
    Genet Couns; 1999 Jan 16; 10(3):325-7. PubMed ID: 10546107
    [Abstract] [Full Text] [Related]

  • 14. Interstitial deletion of 4(q21q25) in a liveborn male.
    Rose NC, Schneider A, McDonald-McGinn DM, Caserta C, Emanuel BS, Zackai EH.
    Am J Med Genet; 1991 Jul 01; 40(1):77-9. PubMed ID: 1887853
    [Abstract] [Full Text] [Related]

  • 15. An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
    Bremer A, Schoumans J, Nordenskjöld M, Anderlid BM, Giacobini M.
    Eur J Med Genet; 2009 Jul 01; 52(5):358-62. PubMed ID: 19576304
    [Abstract] [Full Text] [Related]

  • 16. Terminal deletion of long arm of chromosome 4: patient report and literature review.
    Evers LJ, Schrander-Stumpel CT, Engelen JJ, Mulder H, Borghgraef M, Fryns JP.
    Genet Couns; 1993 Jul 01; 4(2):139-45. PubMed ID: 7689326
    [Abstract] [Full Text] [Related]

  • 17. Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies.
    Zenger-Hain JL, Roberson J, Van Dyke DL, Weiss L.
    Am J Med Genet; 1993 Jun 01; 46(4):438-40. PubMed ID: 7689299
    [Abstract] [Full Text] [Related]

  • 18. Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)].
    Chitayat D, Babul R, Silver MM, Jay V, Teshima IE, Babyn P, Becker LE.
    Am J Med Genet; 1996 Jan 02; 61(1):45-8. PubMed ID: 8741917
    [Abstract] [Full Text] [Related]

  • 19. De novo 10q22 interstitial deletion.
    Cook L, Weaver DD, Hartsfield JK, Vance GH.
    J Med Genet; 1999 Jan 02; 36(1):71-2. PubMed ID: 9950372
    [Abstract] [Full Text] [Related]

  • 20. Deletion of the long arm of chromosome 4 [46,XX,del(4)(q31)] in a patient with congenital anomalies.
    Back E, Hertel C, Vogel W, Bettecken F, Thiesen M.
    Ann Genet; 1977 Dec 02; 20(4):294-6. PubMed ID: 305761
    [Abstract] [Full Text] [Related]

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