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Journal Abstract Search

75 related items for PubMed ID: 17022583

  • 21. Autism and Williams syndrome: a case report.
    Herguner S, Mukaddes NM.
    World J Biol Psychiatry; 2006; 7(3):186-8. PubMed ID: 16861145
    [Abstract] [Full Text] [Related]

  • 22. Williams Syndrome with Infantile Spasms.
    Polat İ, Karaoglu P, Ayanoglu M, Yis U, Hiz S.
    Indian J Pediatr; 2015 Aug; 82(8):757-8. PubMed ID: 25772942
    [No Abstract] [Full Text] [Related]

  • 23. Prenatal diagnosis of a fetus with 7q11.23 deletion detected by multiplex ligation-dependent probe amplification (MLPA) screening.
    Kontos H, Manolakos E, Malligiannis P, Plachouras N, Ploumis N, Mihalatos M, Orru S, Anastasiadou E, Petersen MB.
    Prenat Diagn; 2008 Jun; 28(6):556-8. PubMed ID: 18509863
    [No Abstract] [Full Text] [Related]

  • 24. Clinical utility gene card for: Williams-Beuren Syndrome [7q11.23].
    Koehler U, Pabst B, Pober B, Kozel B.
    Eur J Hum Genet; 2014 Sep; 22(9):. PubMed ID: 24569604
    [No Abstract] [Full Text] [Related]

  • 25. Further clinical description of duplication of Williams-Beuren region presenting with congenital glaucoma and brachycephaly.
    Merritt JL, Lindor NM.
    Am J Med Genet A; 2008 Apr 15; 146A(8):1055-8. PubMed ID: 18266245
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  • 28. Diagnosis of DiGeorge and Williams syndromes using FISH analysis of peripheral blood smears.
    Novelli A, Sabani M, Caiola A, Digilio MC, Giannotti A, Mingarelli R, Novelli G, Dallapiccola B.
    Mol Cell Probes; 1999 Aug 15; 13(4):303-7. PubMed ID: 10441203
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  • 33. A 22-month-old boy with slow development.
    Charrow J.
    Pediatr Ann; 2005 Apr 15; 34(4):270, 273. PubMed ID: 15871431
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  • 35. Supernumerary nipples--a new finding in Williams syndrome.
    Moore RS, Morrison PJ.
    Clin Dysmorphol; 2016 Apr 15; 25(2):84-5. PubMed ID: 26862942
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  • 36. The mystery of sudden death in Williams-Beuren syndrome: cardiomyopathy or Kounis syndrome?
    Kounis NG, Soufras GD, Mazarakis A.
    Int J Cardiol; 2012 May 03; 156(3):251-2. PubMed ID: 22078390
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