BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

174 related articles for article (PubMed ID: 26012727)

  • 21. The clinical course of an overgrowth syndrome, from diagnosis in infancy through adulthood: the case of Beckwith-Wiedemann syndrome.
    Pappas JG
    Curr Probl Pediatr Adolesc Health Care; 2015 Apr; 45(4):112-7. PubMed ID: 25861997
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15: few clinical features suggestive of Beckwith-Wiedemann syndrome.
    Adachi H; Takahashi I; Higashimoto K; Tsuchida S; Noguchi A; Tamura H; Arai H; Ito T; Masue M; Nishibori H; Takahashi T; Soejima H
    Endocr J; 2013; 60(4):403-8. PubMed ID: 23197114
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted.
    Weksberg R; Teshima I; Williams BR; Greenberg CR; Pueschel SM; Chernos JE; Fowlow SB; Hoyme E; Anderson IJ; Whiteman DA
    Hum Mol Genet; 1993 May; 2(5):549-56. PubMed ID: 8518793
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 3p partial trisomy and 13q partial monosomy with congenital malformations and psychomotor developmental delay.
    Rodovalho-Doriqui MJ; Freitas PL; Pinho JD; Cavalli LR; Pereira SR
    Genet Mol Res; 2013 Jul; 12(3):2562-6. PubMed ID: 23979887
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Characterization of the breakpoints in unbalanced t(5;11)(p15;p15) constitutional chromosome translocations in two patients with beckwith-wiedemann syndrome using fluorescence in situ hybridisation.
    Grundy RG; Aledo R; Cowell JK
    Int J Mol Med; 1998 May; 1(5):801-8. PubMed ID: 9852299
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Uniparental disomy of chromosome 11 in a patient with Beckwith-Wiedemann syndrome. First reported case in Iceland].
    Pálsson GI; Finnsdóttir V; Jóhannsson JH; Ingvarsson S
    Laeknabladid; 2005 Nov; 91(11):837-40. PubMed ID: 16264244
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome.
    Slavotinek A; Gaunt L; Donnai D
    J Med Genet; 1997 Oct; 34(10):819-26. PubMed ID: 9350814
    [TBL] [Abstract][Full Text] [Related]  

  • 28. New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome.
    Smith AC; Rubin T; Shuman C; Estabrooks L; Aylsworth AS; McDonald MT; Steele L; Ray PN; Weksberg R
    Cytogenet Genome Res; 2006; 113(1-4):313-7. PubMed ID: 16575195
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Factor VII deficiency and developmental abnormalities in a patient with partial monosomy of 13q and trisomy of 16p: case report and review of the literature.
    Brooks BP; Meck JM; Haddad BR; Bendavid C; Blain D; Toretsky JA
    BMC Med Genet; 2006 Jan; 7():2. PubMed ID: 16412230
    [TBL] [Abstract][Full Text] [Related]  

  • 30. MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment.
    Priolo M; Sparago A; Mammì C; Cerrato F; Laganà C; Riccio A
    Eur J Hum Genet; 2008 May; 16(5):565-71. PubMed ID: 18212817
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci.
    Azzi S; Rossignol S; Steunou V; Sas T; Thibaud N; Danton F; Le Jule M; Heinrichs C; Cabrol S; Gicquel C; Le Bouc Y; Netchine I
    Hum Mol Genet; 2009 Dec; 18(24):4724-33. PubMed ID: 19755383
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases.
    Turleau C; de Grouchy J; Chavin-Colin F; Martelli H; Voyer M; Charlas R
    Hum Genet; 1984; 67(2):219-21. PubMed ID: 6745943
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular biology of Beckwith-Wiedemann syndrome.
    Weksberg R; Squire JA
    Med Pediatr Oncol; 1996 Nov; 27(5):462-9. PubMed ID: 8827075
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5).
    Tommerup N; Brandt CA; Pedersen S; Bolund L; Kamper J
    J Med Genet; 1993 Nov; 30(11):958-61. PubMed ID: 8301654
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
    Sohn YB; Yun JN; Park SJ; Park MS; Kim SH; Lee JH
    Ann Clin Lab Sci; 2013; 43(3):332-6. PubMed ID: 23884231
    [TBL] [Abstract][Full Text] [Related]  

  • 36. De novo paternal origin duplication of chromosome 11p15.5: report of two Chinese cases with Beckwith-Wiedemann syndrome.
    Wang Q; Geng Q; Zhou Q; Luo F; Li P; Xie J
    Mol Cytogenet; 2017; 10():46. PubMed ID: 29270226
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Bilateral Cleft Lip and Palate Accompanied by 13q- Syndrome with Deficiencies of FVII and FX: A Case Report.
    Mishima K; Shiraishi M; Umeda H
    J Clin Pediatr Dent; 2019; 43(4):288-291. PubMed ID: 31094634
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Genetic analysis of two pediatric patients with Beckwith-Wiedemann syndrome].
    Li X; Lyu Y; Gao M; Yan X; Meng C; Zhang K; Liu Y; Gai Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec; 34(6):831-834. PubMed ID: 29188610
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Nonimmune fetal hydrops and placentomegaly: diagnosis of familial Wiedemann-Beckwith syndrome with trisomy 11p15 using FISH.
    Drut RM; Drut R
    Am J Med Genet; 1996 Mar; 62(2):145-9. PubMed ID: 8882394
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Microarray detection of a de novo der(X)t(X;11)(q28;p13) in a girl with premature ovarian failure and features of Beckwith-Wiedemann syndrome.
    Han JY; Shin JH; Han MS; Je GH; Shaffer LG
    J Hum Genet; 2006; 51(7):641-3. PubMed ID: 16708166
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.