BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

248 related articles for article (PubMed ID: 26012591)

  • 1. Polymicrogyria in a 10-month-old boy with Mowat-Wilson syndrome.
    Murray SB; Spangler BB; Helm BM; Vergano SS
    Am J Med Genet A; 2015 Oct; 167A(10):2402-5. PubMed ID: 26012591
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 164A(8):1899-908. PubMed ID: 24715670
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The behavioral phenotype of Mowat-Wilson syndrome.
    Evans E; Einfeld S; Mowat D; Taffe J; Tonge B; Wilson M
    Am J Med Genet A; 2012 Feb; 158A(2):358-66. PubMed ID: 22246645
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 164A(10):2557-66. PubMed ID: 25123255
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sleep disturbance in Mowat-Wilson syndrome.
    Evans E; Mowat D; Wilson M; Einfeld S
    Am J Med Genet A; 2016 Mar; 170(3):654-60. PubMed ID: 26686679
    [TBL] [Abstract][Full Text] [Related]  

  • 6. ZEB2 gene mutation and duplication of 22q11.23 in Mowat-Wilson syndrome.
    Buraniqi E; Moodley M
    J Child Neurol; 2015 Jan; 30(1):32-6. PubMed ID: 25028418
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel Zeb2 gene variation in the Mowat Wilson syndrome (MWS).
    Moore SW; Fieggen K; Honey E; Zaahl M
    J Pediatr Surg; 2016 Feb; 51(2):268-71. PubMed ID: 26852091
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical spectrum of eye malformations in four patients with Mowat-Wilson syndrome.
    Bourchany A; Giurgea I; Thevenon J; Goldenberg A; Morin G; Bremond-Gignac D; Paillot C; Lafontaine PO; Thouvenin D; Massy J; Duncombe A; Thauvin-Robinet C; Masurel-Paulet A; Chehadeh SE; Huet F; Bron A; Creuzot-Garcher C; Lyonnet S; Faivre L
    Am J Med Genet A; 2015 Jul; 167(7):1587-92. PubMed ID: 25899569
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mowat-Wilson syndrome presenting with fever-associated seizures.
    Seo SE; Kim SH; Lee ST; Choi JR; Lee JS; Kim HD; Kang HC
    Epileptic Disord; 2017 Dec; 19(4):481-485. PubMed ID: 29258970
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical utility gene card for: Mowat-Wilson syndrome.
    Zollino M; Garavelli L; Rauch A
    Eur J Hum Genet; 2011 Aug; 19(8):. PubMed ID: 21343952
    [No Abstract]   [Full Text] [Related]  

  • 11. [Mowat-Wilson syndrome: a report of three Danish cases].
    Nissen KB; Søndergaard C; Thelle T; Møller RS
    Ugeskr Laeger; 2011 Sep; 173(36):2199-200. PubMed ID: 21893004
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mowat-Wilson syndrome associated with craniosynostosis.
    Hartill VL; Pendlebury M; Hobson E
    Clin Dysmorphol; 2014 Jan; 23(1):16-19. PubMed ID: 24300291
    [No Abstract]   [Full Text] [Related]  

  • 13. Ophthalmologic abnormalities in Mowat-Wilson syndrome and a mutation in ZEB2.
    Ariss M; Natan K; Friedman N; Traboulsi EI
    Ophthalmic Genet; 2012 Sep; 33(3):159-60. PubMed ID: 22486326
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mowat-Wilson syndrome.
    Mowat DR; Wilson MJ; Goossens M
    J Med Genet; 2003 May; 40(5):305-10. PubMed ID: 12746390
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Recurrence of Mowat-Wilson syndrome in siblings with the same proven mutation.
    McGaughran J; Sinnott S; Dastot-Le Moal F; Wilson M; Mowat D; Sutton B; Goossens M
    Am J Med Genet A; 2005 Sep; 137A(3):302-4. PubMed ID: 16088920
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A missense mutation in the ZFHX1B gene associated with an atypical Mowat-Wilson syndrome phenotype.
    Heinritz W; Zweier C; Froster UG; Strenge S; Kujat A; Syrbe S; Rauch A; Schuster V
    Am J Med Genet A; 2006 Jun; 140(11):1223-7. PubMed ID: 16688751
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neuropathology of Mowat-Wilson Syndrome.
    Conces MR; Hughes A; Pierson CR
    Pediatr Dev Pathol; 2020 Aug; 23(4):322-325. PubMed ID: 32252596
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literature.
    Garavelli L; Zollino M; Mainardi PC; Gurrieri F; Rivieri F; Soli F; Verri R; Albertini E; Favaron E; Zignani M; Orteschi D; Bianchi P; Faravelli F; Forzano F; Seri M; Wischmeijer A; Turchetti D; Pompilii E; Gnoli M; Cocchi G; Mazzanti L; Bergamaschi R; De Brasi D; Sperandeo MP; Mari F; Uliana V; Mostardini R; Cecconi M; Grasso M; Sassi S; Sebastio G; Renieri A; Silengo M; Bernasconi S; Wakamatsu N; Neri G
    Am J Med Genet A; 2009 Mar; 149A(3):417-26. PubMed ID: 19215041
    [TBL] [Abstract][Full Text] [Related]  

  • 19. ZEB2 zinc-finger missense mutations lead to hypomorphic alleles and a mild Mowat-Wilson syndrome.
    Ghoumid J; Drevillon L; Alavi-Naini SM; Bondurand N; Rio M; Briand-Suleau A; Nasser M; Goodwin L; Raymond P; Yanicostas C; Goossens M; Lyonnet S; Mowat D; Amiel J; Soussi-Yanicostas N; Giurgea I
    Hum Mol Genet; 2013 Jul; 22(13):2652-61. PubMed ID: 23466526
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mowat-Wilson syndrome in a fetus with antenatal diagnosis of short corpus callosum: advocacy for standard autopsy.
    Spaggiari E; Baumann C; Alison M; Oury JF; Belarbi N; Dupont C; Guimiot F; Delezoide AL
    Eur J Med Genet; 2013 Jun; 56(6):297-300. PubMed ID: 23523603
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.