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 *

125 related articles for article (PubMed ID: 17593542)

  • 21. Is maternal duplication of 11p15 associated with Silver-Russell syndrome?
    Eggermann T; Meyer E; Obermann C; Heil I; Schüler H; Ranke MB; Eggermann K; Wollmann HA
    J Med Genet; 2005 May; 42(5):e26. PubMed ID: 15863658
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Placental mesenchymal dysplasia: An underdiagnosed placental pathology with various clinical outcomes.
    Guenot C; Kingdom J; De Rham M; Osterheld M; Keating S; Vial Y; Van Mieghem T; Jastrow N; Raio L; Spinelli M; Di Meglio L; Chalouhi G; Baud D
    Eur J Obstet Gynecol Reprod Biol; 2019 Mar; 234():155-164. PubMed ID: 30703717
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Uniparental paternal disomy in a genetic cancer-predisposing syndrome.
    Henry I; Bonaiti-Pellié C; Chehensse V; Beldjord C; Schwartz C; Utermann G; Junien C
    Nature; 1991 Jun; 351(6328):665-7. PubMed ID: 1675767
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Placental mesenchymal dysplasia is associated with high rates of intrauterine growth restriction and fetal demise: A report of 11 new cases and a review of the literature.
    Pham T; Steele J; Stayboldt C; Chan L; Benirschke K
    Am J Clin Pathol; 2006 Jul; 126(1):67-78. PubMed ID: 16753607
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Biparental/androgenetic mosaicism in a male with features of overgrowth and placental mesenchymal dysplasia.
    Repnikova E; Roberts J; Kats A; Habeebu S; Schwager C; Joyce J; Manalang M; Amudhavalli SM
    Clin Genet; 2018 Dec; 94(6):564-568. PubMed ID: 30084132
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Fibroadenoma in Beckwith-Wiedemann syndrome with paternal uniparental disomy of chromosome 11p15.5.
    Takama Y; Kubota A; Nakayama M; Higashimoto K; Jozaki K; Soejima H
    Pediatr Int; 2014 Dec; 56(6):931-934. PubMed ID: 25521982
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Severe presentation of Beckwith-Wiedemann syndrome associated with high levels of constitutional paternal uniparental disomy for chromosome 11p15.
    Smith AC; Shuman C; Chitayat D; Steele L; Ray PN; Bourgeois J; Weksberg R
    Am J Med Genet A; 2007 Dec; 143A(24):3010-5. PubMed ID: 18000906
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Placental mesenchymal dysplasia with beckwith-wiedemann syndrome fetus in the context of biparental and androgenic cell lines.
    H'mida D; Gribaa M; Yacoubi T; Chaieb A; Adala L; Elghezal H; Saad A
    Placenta; 2008 May; 29(5):454-60. PubMed ID: 18342934
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mosaic paternal genome-wide uniparental isodisomy with down syndrome.
    Darcy D; Atwal PS; Angell C; Gadi I; Wallerstein R
    Am J Med Genet A; 2015 Oct; 167A(10):2463-9. PubMed ID: 26219535
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Placental mesenchymal dysplasia with a good outcome: A case report.
    Oide S; Kuwata T; Wang L; Imai K; Chikazawa K; Takagi K
    J Obstet Gynaecol Res; 2019 Nov; 45(11):2284-2288. PubMed ID: 31448853
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 11p15 duplication and 13q34 deletion with Beckwith-Wiedemann syndrome and factor VII deficiency.
    Jurkiewicz D; Kugaudo M; Tańska A; Wawrzkiewicz-Witkowska A; Tomaszewska A; Kucharczyk M; Cieślikowska A; Ciara E; Krajewska-Walasek M
    Pediatr Int; 2015 Jun; 57(3):486-91. PubMed ID: 26012727
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.
    Catchpoole D; Lam WW; Valler D; Temple IK; Joyce JA; Reik W; Schofield PN; Maher ER
    J Med Genet; 1997 May; 34(5):353-9. PubMed ID: 9152830
    [TBL] [Abstract][Full Text] [Related]  

  • 35. SNP arrays in Beckwith-Wiedemann syndrome: an improved diagnostic strategy.
    Keren B; Chantot-Bastaraud S; Brioude F; Mach C; Fonteneau E; Azzi S; Depienne C; Brice A; Netchine I; Le Bouc Y; Siffroi JP; Rossignol S
    Eur J Med Genet; 2013 Oct; 56(10):546-50. PubMed ID: 23892181
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Placental Pathology in Beckwith-Wiedemann Syndrome According to Genotype/Epigenotype Subgroups.
    Gaillot-Durand L; Brioude F; Beneteau C; Le Breton F; Massardier J; Michon L; Devouassoux-Shisheboran M; Allias F
    Fetal Pediatr Pathol; 2018 Dec; 37(6):387-399. PubMed ID: 30633605
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prenatal diagnosis of paternal duplication of 11p15.5→14.3: Its implication of Beckwith-Wiedemann syndrome.
    Chen KJ; Liu YM; Li CH; Chang YL; Chang SD
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):877-880. PubMed ID: 28040139
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism.
    Chen CP; Tsai C; Lin MH; Chern SR; Chen SW; Lai ST; Chen WL; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Oct; 56(5):691-693. PubMed ID: 29037560
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [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]  

  • 40. Assessment of p57(KIP2) gene mutation in Beckwith-Wiedemann syndrome.
    Gaston V; Le Bouc Y; Soupre V; Vazquez MP; Gicquel C
    Horm Res; 2000; 54(1):1-5. PubMed ID: 11182628
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.