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Journal Abstract Search

137 related items for PubMed ID: 38154310

  • 1. Fatal cardiac dysfunction in a child with Williams syndrome.
    Kawai C, Kondo H, Miyao M, Sunada M, Ozawa S, Kotani H, Minami H, Nagai H, Abiru H, Yamamoto A, Tamaki K, Nishitani Y.
    Leg Med (Tokyo); 2024 Mar; 67():102387. PubMed ID: 38154310
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  • 3. [Williams syndrome].
    Ohashi H.
    Nihon Rinsho; 2005 Jul; 63(7):1185-9. PubMed ID: 16001780
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  • 4. An Update on Common Chromosome Microdeletion and Microduplication Syndromes.
    Goldenberg P.
    Pediatr Ann; 2018 May 01; 47(5):e198-e203. PubMed ID: 29750287
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  • 6. Death following tonsillectomy in a child with Williams syndrome.
    Monfared A, Messner A.
    Int J Pediatr Otorhinolaryngol; 2006 Jun 01; 70(6):1133-5. PubMed ID: 16406078
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  • 7. An unusual combination of an atypical maternally inherited novel 0.3 Mb deletion in Williams-Beuren region and a de novo 22q11.21 microduplication in an infant with supravalvular aortic stenosis.
    Evangelidou P, Kousoulidou L, Salameh N, Alexandrou A, Papaevripidou I, Alexandrou IM, Ketoni A, Ioannidou C, Christophidou-Anastasiadou V, Tanteles GA, Sismani C.
    Eur J Med Genet; 2020 Dec 01; 63(12):104084. PubMed ID: 33045407
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  • 9. Molecular cytogenetic diagnosis of Williams syndrome.
    Hirota H, Matsuoka R, Kimura M, Imamura S, Joh-o K, Ando M, Takao A, Momma K.
    Am J Med Genet; 1996 Aug 23; 64(3):473-7. PubMed ID: 8862624
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  • 12. An infant with suspected missed diagnosis of Williams syndrome failed weaning off CPB after surgical correction of pulmonary stenosis: a case report and literature review.
    Yuan Y, Zhou R.
    Perfusion; 2023 Jan 23; 38(1):203-207. PubMed ID: 34538195
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  • 15. Neonatal Williams syndrome presenting as an isolated supravalvular pulmonary stenosis.
    di Gioia CR, Ciallella C, d'Amati G, Parroni E, Nardone AM, Gallo P.
    Arch Pathol Lab Med; 2003 Sep 23; 127(9):e367-70. PubMed ID: 12946215
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  • 17. Microdeletion oe chromosomal region 7Q11.23 in Williams syndrome.
    Hou JW, Wang JK, Wang TR.
    J Formos Med Assoc; 1997 Feb 23; 96(2):137-40. PubMed ID: 9071842
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  • 18. Congenital heart defects in Williams syndrome.
    Yuan SM.
    Turk J Pediatr; 2017 Feb 23; 59(3):225-232. PubMed ID: 29376566
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  • 19. 16p11.2 microdeletion syndrome: a case report.
    Dell'Edera D, Dilucca C, Allegretti A, Simone F, Lupo MG, Liccese C, Davanzo R.
    J Med Case Rep; 2018 Apr 03; 12(1):90. PubMed ID: 29609622
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  • 20. GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region.
    Morris CA, Mervis CB, Hobart HH, Gregg RG, Bertrand J, Ensing GJ, Sommer A, Moore CA, Hopkin RJ, Spallone PA, Keating MT, Osborne L, Kimberley KW, Stock AD.
    Am J Med Genet A; 2003 Nov 15; 123A(1):45-59. PubMed ID: 14556246
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