BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 27831545)

  • 41. Mowat-Wilson syndrome detected by using high resolution microarray.
    Park JY; Cho EH; Lee EH; Kang YS; Jun KR; Hur YJ
    Gene; 2013 Dec; 532(2):307-9. PubMed ID: 24029077
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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]  

  • 43. Mowat Wilson syndrome and Hirschsprung disease: a retrospective study on functional outcomes.
    Dagorno C; Pio L; Capri Y; Ali L; Giurgea I; Qoshe L; Morcrette G; Julien-Marsollier F; Sommet J; Chomton M; Berrebi D; Bonnard A
    Pediatr Surg Int; 2020 Nov; 36(11):1309-1315. PubMed ID: 32980962
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Generation of two iPSC lines from Mowat-Wilson syndrome patients carrying heterozygous ZEB2 mutations.
    Gorrieri G; Tamburro S; Baldassari S; Guerrisi S; Zara F; Ricci E; Maria Cordelli D; Scudieri P; Musante I
    Stem Cell Res; 2024 Apr; 76():103333. PubMed ID: 38350246
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Clinical features and management issues in Mowat-Wilson syndrome.
    Adam MP; Schelley S; Gallagher R; Brady AN; Barr K; Blumberg B; Shieh JT; Graham J; Slavotinek A; Martin M; Keppler-Noreuil K; Storm AL; Hudgins L
    Am J Med Genet A; 2006 Dec; 140(24):2730-41. PubMed ID: 17103451
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Congenital tracheal stenosis in Mowat-Wilson syndrome with nonsense mutation of ZEB2 gene.
    Lin LC; Wen WH; Chen PT
    Pediatr Neonatol; 2024 Mar; 65(2):202-203. PubMed ID: 37980276
    [No Abstract]   [Full Text] [Related]  

  • 47. Early Infantile Epileptic Encephalopathy with a de novo variant in ZEB2 identified by exome sequencing.
    Babkina N; Deignan JL; Lee H; Vilain E; Sankar R; Giurgea I; Mowat D; Graham JM
    Eur J Med Genet; 2016 Feb; 59(2):70-4. PubMed ID: 26721324
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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]  

  • 49. Mowat-Wilson syndrome: neurological and molecular study in seven patients.
    Paz JA; Kim CA; Goossens M; Giurgea I; Marques-Dias MJ
    Arq Neuropsiquiatr; 2015 Jan; 73(1):12-7. PubMed ID: 25608121
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Severe clinical course of Hirschsprung disease in a Mowat-Wilson syndrome patient.
    Smigiel R; Szafranska A; Czyzewska M; Rauch A; Zweier Ch; Patkowski D
    J Appl Genet; 2010; 51(1):111-3. PubMed ID: 20145308
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Clinical and genetic features of Mowat-Wilson syndrome: an analysis of 3 cases].
    Wang H; Yan YC; Li Q; Zhang Z; Xiao P; Yuan XY; Li L; Jiang Q
    Zhongguo Dang Dai Er Ke Za Zhi; 2019 May; 21(5):468-473. PubMed ID: 31104665
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Identification of MMACHC and ZEB2 mutations causing coexistent cobalamin C disease and Mowat-Wilson syndrome in a 2-year-old girl.
    Liu F; Wu Y; Li Z; Wan R
    Clin Chim Acta; 2022 Aug; 533():31-39. PubMed ID: 35709987
    [TBL] [Abstract][Full Text] [Related]  

  • 53. 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]  

  • 54. De novo inbred heterozygous Zeb2/Sip1 mutant mice uniquely generated by germ-line conditional knockout exhibit craniofacial, callosal and behavioral defects associated with Mowat-Wilson syndrome.
    Takagi T; Nishizaki Y; Matsui F; Wakamatsu N; Higashi Y
    Hum Mol Genet; 2015 Nov; 24(22):6390-402. PubMed ID: 26319231
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Targeted chromatin conformation analysis identifies novel distal neural enhancers of ZEB2 in pluripotent stem cell differentiation.
    Birkhoff JC; Brouwer RWW; Kolovos P; Korporaal AL; Bermejo-Santos A; Boltsis I; Nowosad K; van den Hout MCGN; Grosveld FG; van IJcken WFJ; Huylebroeck D; Conidi A
    Hum Mol Genet; 2020 Aug; 29(15):2535-2550. PubMed ID: 32628253
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [Clinical features of epilepsy in 5 children with Mowat-Wilson syndrome].
    Ju Y; Ji TY
    Zhonghua Er Ke Za Zhi; 2022 Jun; 60(6):578-582. PubMed ID: 35658366
    [No Abstract]   [Full Text] [Related]  

  • 57. [Analysis of a case with Mowat-Wilson syndrome due to nonsense variant of ZEB2 gene].
    She M; Zhao Z; Shi P; Gao S; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Aug; 39(8):889-892. PubMed ID: 35929943
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Mowat-Wilson syndrome: the first two Malaysian cases.
    Balasubramaniam S; Keng WT; Ngu LH; Michel LG; Irina G
    Singapore Med J; 2010 Mar; 51(3):e54-7. PubMed ID: 20428734
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Ocular phenotype of Mowat-Wilson syndrome in the first reported Cypriot patients: an under-recognized association.
    Tanteles GA; Christophidou-Anastasiadou V
    Clin Dysmorphol; 2014 Jan; 23(1):20-23. PubMed ID: 24263623
    [No Abstract]   [Full Text] [Related]  

  • 60.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.