These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 38228391)

  • 21. Clinical and molecular features of children with Beckwith-Wiedemann syndrome in China: a single-center retrospective cohort study.
    Wang R; Xiao Y; Li D; Hu H; Li X; Ge T; Yu R; Wang Y; Zhang T
    Ital J Pediatr; 2020 Apr; 46(1):55. PubMed ID: 32349794
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prenatal findings and the genetic diagnosis of fetal overgrowth disorders: Simpson-Golabi-Behmel syndrome, Sotos syndrome, and Beckwith-Wiedemann syndrome.
    Chen CP
    Taiwan J Obstet Gynecol; 2012 Jun; 51(2):186-91. PubMed ID: 22795092
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.
    Russo S; Calzari L; Mussa A; Mainini E; Cassina M; Di Candia S; Clementi M; Guzzetti S; Tabano S; Miozzo M; Sirchia S; Finelli P; Prontera P; Maitz S; Sorge G; Calcagno A; Maghnie M; Divizia MT; Melis D; Manfredini E; Ferrero GB; Pecile V; Larizza L
    Clin Epigenetics; 2016; 8():23. PubMed ID: 26933465
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetic considerations in the prenatal diagnosis of overgrowth syndromes.
    Vora N; Bianchi DW
    Prenat Diagn; 2009 Oct; 29(10):923-9. PubMed ID: 19609940
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Silver-Russell and Beckwith-Wiedemann syndromes: opposite (epi)mutations in 11p15 result in opposite clinical pictures.
    Eggermann T
    Horm Res; 2009 Apr; 71 Suppl 2():30-5. PubMed ID: 19407494
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith-Wiedemann syndrome.
    Lin HY; Chuang CK; Tu RY; Fang YY; Su YN; Chen CP; Chang CY; Liu HC; Chu TH; Niu DM; Lin SP
    Mol Genet Metab; 2016 Sep; 119(1-2):8-13. PubMed ID: 27436784
    [TBL] [Abstract][Full Text] [Related]  

  • 27. High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith-Wiedemann syndrome.
    Baskin B; Choufani S; Chen YA; Shuman C; Parkinson N; Lemyre E; Micheil Innes A; Stavropoulos DJ; Ray PN; Weksberg R
    Hum Genet; 2014 Mar; 133(3):321-30. PubMed ID: 24154661
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important.
    Eggermann T; Brück J; Knopp C; Fekete G; Kratz C; Tasic V; Kurth I; Elbracht M; Eggermann K; Begemann M
    J Mol Med (Berl); 2020 Oct; 98(10):1447-1455. PubMed ID: 32839827
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. A novel IGF2/H19 domain triplication in the 11p15.5 imprinting region causing either Beckwith-Wiedemann or Silver-Russell syndrome in a single family.
    Jurkiewicz D; Kugaudo M; Skórka A; Śmigiel R; Smyk M; Ciara E; Chrzanowska K; Krajewska-Walasek M
    Am J Med Genet A; 2017 Jan; 173(1):72-78. PubMed ID: 27612309
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith-Wiedemann Syndrome: Clinical Spectrum and Functional Characterization.
    Brioude F; Netchine I; Praz F; Le Jule M; Calmel C; Lacombe D; Edery P; Catala M; Odent S; Isidor B; Lyonnet S; Sigaudy S; Leheup B; Audebert-Bellanger S; Burglen L; Giuliano F; Alessandri JL; Cormier-Daire V; Laffargue F; Blesson S; Coupier I; Lespinasse J; Blanchet P; Boute O; Baumann C; Polak M; Doray B; Verloes A; Viot G; Le Bouc Y; Rossignol S
    Hum Mutat; 2015 Sep; 36(9):894-902. PubMed ID: 26077438
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Investigation of 11p15.5 Methylation Defects Associated with Beckwith-Wiedemann Spectrum and Embryonic Tumor Risk in Lateralized Overgrowth Patients.
    Tüysüz B; Bozlak S; Uludağ Alkaya D; Ocak S; Kasap B; Sunamak Çifçi E; Seker A; Bayhan IA; Apak H
    Cancers (Basel); 2023 Mar; 15(6):. PubMed ID: 36980758
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Clinical and Molecular Diagnosis of Beckwith-Wiedemann Syndrome with Single- or Multi-Locus Imprinting Disturbance.
    Fontana L; Tabano S; Maitz S; Colapietro P; Garzia E; Gerli AG; Sirchia SM; Miozzo M
    Int J Mol Sci; 2021 Mar; 22(7):. PubMed ID: 33810554
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A 4-Year-Old Boy with Beckwith Wiedemann Syndrome (BWS).
    Janchevska A; Tasic V; Laban N; Polenakovic M; Gucev Z; Bachmann N; Bergmann C
    Pril (Makedon Akad Nauk Umet Odd Med Nauki); 2018 Dec; 39(2-3):131-135. PubMed ID: 30864369
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance.
    Cubellis MV; Pignata L; Verma A; Sparago A; Del Prete R; Monticelli M; Calzari L; Antona V; Melis D; Tenconi R; Russo S; Cerrato F; Riccio A
    Clin Epigenetics; 2020 Sep; 12(1):139. PubMed ID: 32928291
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Variable Expressivity of the Beckwith-Wiedemann Syndrome in Four Pedigrees Segregating Loss-of-Function Variants of
    Sparago A; Cerrato F; Pignata L; Cammarata-Scalisi F; Garavelli L; Piscopo C; Vancini A; Riccio A
    Genes (Basel); 2021 May; 12(5):. PubMed ID: 34065128
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.
    Weksberg R; Nishikawa J; Caluseriu O; Fei YL; Shuman C; Wei C; Steele L; Cameron J; Smith A; Ambus I; Li M; Ray PN; Sadowski P; Squire J
    Hum Mol Genet; 2001 Dec; 10(26):2989-3000. PubMed ID: 11751681
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Diagnosis of Beckwith-Wiedemann syndrome in children presenting with Wilms tumor.
    MacFarland SP; Duffy KA; Bhatti TR; Bagatell R; Balamuth NJ; Brodeur GM; Ganguly A; Mattei PA; Surrey LF; Balis FM; Kalish JM
    Pediatr Blood Cancer; 2018 Oct; 65(10):e27296. PubMed ID: 29932284
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Clinical and molecular overlap in overgrowth syndromes.
    Baujat G; Rio M; Rossignol S; Sanlaville D; Lyonnet S; Le Merrer M; Munnich A; Gicquel C; Colleaux L; Cormier-Daire V
    Am J Med Genet C Semin Med Genet; 2005 Aug; 137C(1):4-11. PubMed ID: 16010674
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Diagnosis and management of the phenotypic spectrum of twins with Beckwith-Wiedemann syndrome.
    Cohen JL; Duffy KA; Sajorda BJ; Hathaway ER; Gonzalez-Gandolfi CX; Richards-Yutz J; Gunter AT; Ganguly A; Kaplan J; Deardorff MA; Kalish JM
    Am J Med Genet A; 2019 Jul; 179(7):1139-1147. PubMed ID: 31067005
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.