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Journal Abstract Search

135 related items for PubMed ID: 39029032

  • 1. Mowat-Wilson syndrome: Case report.
    Wójcik-Niklewska B, Filipek E.
    Medicine (Baltimore); 2024 Jul 19; 103(29):e39082. PubMed ID: 39029032
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  • 4. CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases.
    Wenger TL, Harr M, Ricciardi S, Bhoj E, Santani A, Adam MP, Barnett SS, Ganetzky R, McDonald-McGinn DM, Battaglia D, Bigoni S, Selicorni A, Sorge G, Monica MD, Mari F, Andreucci E, Romano S, Cocchi G, Savasta S, Malbora B, Marangi G, Garavelli L, Zollino M, Zackai EH.
    Am J Med Genet A; 2014 Oct 19; 164A(10):2557-66. PubMed ID: 25123255
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  • 9. Mowat-Wilson syndrome in a Chinese population: A case series.
    Ho S, Luk HM, Chung BH, Fung JL, Mak HH, Lo IFM.
    Am J Med Genet A; 2020 Jun 19; 182(6):1336-1341. PubMed ID: 32196960
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  • 12. Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care.
    Ivanovski I, Djuric O, Caraffi SG, Santodirocco D, Pollazzon M, Rosato S, Cordelli DM, Abdalla E, Accorsi P, Adam MP, Ajmone PF, Badura-Stronka M, Baldo C, Baldi M, Bayat A, Bigoni S, Bonvicini F, Breckpot J, Callewaert B, Cocchi G, Cuturilo G, De Brasi D, Devriendt K, Dinulos MB, Hjortshøj TD, Epifanio R, Faravelli F, Fiumara A, Formisano D, Giordano L, Grasso M, Grønborg S, Iodice A, Iughetti L, Kuburovic V, Kutkowska-Kazmierczak A, Lacombe D, Lo Rizzo C, Luchetti A, Malbora B, Mammi I, Mari F, Montorsi G, Moutton S, Møller RS, Muschke P, Nielsen JEK, Obersztyn E, Pantaleoni C, Pellicciari A, Pisanti MA, Prpic I, Poch-Olive ML, Raviglione F, Renieri A, Ricci E, Rivieri F, Santen GW, Savasta S, Scarano G, Schanze I, Selicorni A, Silengo M, Smigiel R, Spaccini L, Sorge G, Szczaluba K, Tarani L, Tone LG, Toutain A, Trimouille A, Valera ET, Vergano SS, Zanotta N, Zenker M, Conidi A, Zollino M, Rauch A, Zweier C, Garavelli L.
    Genet Med; 2018 Sep 19; 20(9):965-975. PubMed ID: 29300384
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  • 13. Neuropathology of Mowat-Wilson Syndrome.
    Conces MR, Hughes A, Pierson CR.
    Pediatr Dev Pathol; 2020 Aug 19; 23(4):322-325. PubMed ID: 32252596
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  • 14. A Diagnosis to Consider in Intellectual Disability: Mowat-Wilson Syndrome.
    Kilic E, Cetinkaya A, Utine GE, Boduroğlu K.
    J Child Neurol; 2016 Jun 19; 31(7):913-7. PubMed ID: 26809768
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  • 16. The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations.
    Yamada Y, Nomura N, Yamada K, Matsuo M, Suzuki Y, Sameshima K, Kimura R, Yamamoto Y, Fukushi D, Fukuhara Y, Ishihara N, Nishi E, Imataka G, Suzumura H, Hamano S, Shimizu K, Iwakoshi M, Ohama K, Ohta A, Wakamoto H, Kajita M, Miura K, Yokochi K, Kosaki K, Kuroda T, Kosaki R, Hiraki Y, Saito K, Mizuno S, Kurosawa K, Okamoto N, Wakamatsu N.
    Am J Med Genet A; 2014 Aug 19; 164A(8):1899-908. PubMed ID: 24715670
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  • 17. Unilateral progressive anterior iris adhesions in Mowat-Wilson syndrome: a new ocular finding.
    Hernández-Marrero D, Junaidi RM, Lyons CJ.
    J AAPOS; 2024 Feb 19; 28(1):103807. PubMed ID: 38218547
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  • 20. [Prenatal diagnosis of a fetus with Mowat-Wilson syndrome].
    Hu R, Luo X, Li Y, Lu J, Huang W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Dec 10; 36(12):1203-1205. PubMed ID: 31813148
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