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Journal Abstract Search

104 related items for PubMed ID: 8773902

  • 41. Thrombocytopenia in patients with 22q11.2 deletion syndrome and its association with glycoprotein Ib-beta.
    Kato T, Kosaka K, Kimura M, Imamura S, Yamada O, Iwai K, Ando M, Joh-o K, Kuroe K, Ohtake A, Takao A, Momma K, Matsuoka R.
    Genet Med; 2003; 5(2):113-9. PubMed ID: 12644781
    [Abstract] [Full Text] [Related]

  • 42. [CATCH22 or 22q11 deletion syndrome. An underdiagnosed and misunderstood disease category with a variable clinical picture].
    Oskarsdóttir S, Fasth A, Belfrage M, Viggedal G, Persson C, Eriksson BO.
    Lakartidningen; 1999 Nov 03; 96(44):4789-93. PubMed ID: 10584540
    [Abstract] [Full Text] [Related]

  • 43. Psychiatric inpatients and chromosome deletions within 22q11.2.
    Sugama S, Namihira T, Matsuoka R, Taira N, Eto Y, Maekawa K.
    J Neurol Neurosurg Psychiatry; 1999 Dec 03; 67(6):803-6. PubMed ID: 10567504
    [Abstract] [Full Text] [Related]

  • 44. Scoliosis in velo-cardio-facial syndrome.
    Morava E, Lacassie Y, King A, Illes T, Marble M.
    J Pediatr Orthop; 2002 Dec 03; 22(6):780-3. PubMed ID: 12409907
    [Abstract] [Full Text] [Related]

  • 45. Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci.
    Berend SA, Spikes AS, Kashork CD, Wu JM, Daw SC, Scambler PJ, Shaffer LG.
    Am J Med Genet; 2000 Apr 10; 91(4):313-7. PubMed ID: 10766989
    [Abstract] [Full Text] [Related]

  • 46. The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
    McDonald-McGinn DM, Kirschner R, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Solot C, Wang P, Jacobs I, Handler S, Knightly C, Heher K, Wilson M, Ming JE, Grace K, Driscoll D, Pasquariello P, Randall P, Larossa D, Emanuel BS, Zackai EH.
    Genet Couns; 1999 Apr 10; 10(1):11-24. PubMed ID: 10191425
    [Abstract] [Full Text] [Related]

  • 47. [Small deletion--large effect].
    Lüerssen K, Pruggmayer M, Ptok M.
    HNO; 2004 Mar 10; 52(3):258-60. PubMed ID: 15004686
    [Abstract] [Full Text] [Related]

  • 48. [3 children with velocardiofacial (Shprintzen) syndrome].
    Lie DA, Beemer FA.
    Ned Tijdschr Geneeskd; 1996 Feb 17; 140(7):372-5. PubMed ID: 8628424
    [Abstract] [Full Text] [Related]

  • 49. 4.5 Mb microdeletion in chromosome band 2q33.1 associated with learning disability and cleft palate.
    Urquhart J, Black GC, Clayton-Smith J.
    Eur J Med Genet; 2009 Feb 17; 52(6):454-7. PubMed ID: 19576302
    [Abstract] [Full Text] [Related]

  • 50. Cleft palate, retrognathia and congenital heart disease in velo-cardio-facial syndrome: a phenotype correlation study.
    Friedman MA, Miletta N, Roe C, Wang D, Morrow BE, Kates WR, Higgins AM, Shprintzen RJ.
    Int J Pediatr Otorhinolaryngol; 2011 Sep 17; 75(9):1167-72. PubMed ID: 21763005
    [Abstract] [Full Text] [Related]

  • 51. "CATCH 22" sans cardiac anomaly, thymic hypoplasia, cleft palate, and hypocalcaemia: cAtch 22. A common result of 22q11 deficiency?
    Lipson A, Emanuel B, Colley P, Fagan K, Driscoll DA.
    J Med Genet; 1994 Sep 17; 31(9):741. PubMed ID: 7815448
    [No Abstract] [Full Text] [Related]

  • 52. Morphometry of the head of the caudate nucleus in patients with velocardiofacial syndrome (del 22q11.2).
    Sugama S, Bingham PM, Wang PP, Moss EM, Kobayashi H, Eto Y.
    Acta Paediatr; 2000 May 17; 89(5):546-9. PubMed ID: 10852189
    [Abstract] [Full Text] [Related]

  • 53. 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot.
    Amati F, Mari A, Digilio MC, Mingarelli R, Marino B, Giannotti A, Novelli G, Dallapiccola B.
    Hum Genet; 1995 May 17; 95(5):479-82. PubMed ID: 7759065
    [Abstract] [Full Text] [Related]

  • 54. The velo-cardio-facial syndrome: the otorhinolaryngeal manifestations and implications.
    Vantrappen G, Rommel N, Cremers CW, Devriendt K, Frijns JP.
    Int J Pediatr Otorhinolaryngol; 1998 Oct 02; 45(2):133-41. PubMed ID: 9849681
    [Abstract] [Full Text] [Related]

  • 55. Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders.
    Carlson C, Papolos D, Pandita RK, Faedda GL, Veit S, Goldberg R, Shprintzen R, Kucherlapati R, Morrow B.
    Am J Hum Genet; 1997 Apr 02; 60(4):851-9. PubMed ID: 9106531
    [Abstract] [Full Text] [Related]

  • 56. Clinical characteristics of children with hypoparathyroidism due to 22q11.2 microdeletion.
    Adachi M, Tachibana K, Masuno M, Makita Y, Maesaka H, Okada T, Hizukuri K, Imaizumi K, Kuroki Y, Kurahashi H, Suwa S.
    Eur J Pediatr; 1998 Jan 02; 157(1):34-8. PubMed ID: 9461360
    [Abstract] [Full Text] [Related]

  • 57. Monozygotic twins with 22q11 deletion and discordant phenotypes.
    Fryer A.
    J Med Genet; 1996 Feb 02; 33(2):173. PubMed ID: 8929959
    [No Abstract] [Full Text] [Related]

  • 58. [The relationship between cleft severity and incidence of associated heart defect in children with isolated cleft palate].
    Chen XH, Tang ZD, Sun T.
    Zhonghua Zheng Xing Wai Ke Za Zhi; 2011 Mar 02; 27(2):89-91. PubMed ID: 21774342
    [Abstract] [Full Text] [Related]

  • 59. Cleft palate lateral synechia syndrome without the lateral synechia (CP plus or minus LS syndrome).
    Preus M, Fraser FC, Fuhrmann W.
    Teratology; 1974 Apr 02; 9(2):135-41. PubMed ID: 4824743
    [No Abstract] [Full Text] [Related]

  • 60.
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    [No Abstract] [Full Text] [Related]

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