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 *

568 related articles for article (PubMed ID: 16264244)

  • 1. [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]  

  • 2. Mitotic recombination and uniparental disomy in Beckwith-Wiedemann syndrome.
    Cooper WN; Curley R; Macdonald F; Maher ER
    Genomics; 2007 May; 89(5):613-7. PubMed ID: 17337339
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Proportion of cells with paternal 11p15 uniparental disomy correlates with organ enlargement in Wiedemann-beckwith syndrome.
    Itoh N; Becroft DM; Reeve AE; Morison IM
    Am J Med Genet; 2000 May; 92(2):111-6. PubMed ID: 10797434
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Beckwith-Wiedemann syndrome.
    Weksberg R; Shuman C; Smith AC
    Am J Med Genet C Semin Med Genet; 2005 Aug; 137C(1):12-23. PubMed ID: 16010676
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Diffuse infantile hepatic hemangiomas in a patient with Beckwith-Wiedemann syndrome: A new association?
    Macchiaiolo M; Markowich AH; Diociaiuti A; Gonfiantini MV; Buonuomo PS; Rana I; Monti L; El Hachem M; Bartuli A
    Am J Med Genet A; 2020 Aug; 182(8):1972-1976. PubMed ID: 32573107
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Beckwith-Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques.
    Romanelli V; Meneses HN; Fernández L; Martínez-Glez V; Gracia-Bouthelier R; F Fraga M; Guillén E; Nevado J; Gean E; Martorell L; Marfil VE; García-Miñaur S; Lapunzina P
    Eur J Hum Genet; 2011 Apr; 19(4):416-21. PubMed ID: 21248736
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Quantitative analysis of methylation status at 11p15 and 7q21 for the genetic diagnosis of Beckwith-Wiedemann syndrome and Silver-Russell syndrome.
    Lee BH; Kim GH; Oh TJ; Kim JH; Lee JJ; Choi SH; Lee JY; Kim JM; Choi IH; Kim YM; Choi JH; Yoo HW
    J Hum Genet; 2013 Sep; 58(9):604-10. PubMed ID: 23803580
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Constitutional mosaic genome-wide uniparental disomy due to diploidisation: an unusual cancer-predisposing mechanism.
    Romanelli V; Nevado J; Fraga M; Trujillo AM; Mori MÁ; Fernández L; Pérez de Nanclares G; Martínez-Glez V; Pita G; Meneses H; Gracia R; García-Miñaur S; García de Miguel P; Lecumberri B; Rodríguez JI; González Neira A; Monk D; Lapunzina P
    J Med Genet; 2011 Mar; 48(3):212-6. PubMed ID: 21097775
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Renal abnormalities in beckwith-wiedemann syndrome are associated with 11p15.5 uniparental disomy.
    Goldman M; Smith A; Shuman C; Caluseriu O; Wei C; Steele L; Ray P; Sadowski P; Squire J; Weksberg R; Rosenblum ND
    J Am Soc Nephrol; 2002 Aug; 13(8):2077-84. PubMed ID: 12138139
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome.
    Kubota T; Saitoh S; Matsumoto T; Narahara K; Fukushima Y; Jinno Y; Niikawa N
    Am J Med Genet; 1994 Feb; 49(4):378-83. PubMed ID: 7909196
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver-Russell syndrome.
    Bullman H; Lever M; Robinson DO; Mackay DJ; Holder SE; Wakeling EL
    J Med Genet; 2008 Jun; 45(6):396-9. PubMed ID: 18474587
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [The Wiedemann-Beckwith syndrome and a congenital cataract].
    Momtchilova M; Pelosse B; Laroche L; Vazquez MP
    J Fr Ophtalmol; 2001 May; 24(5):479-81. PubMed ID: 11397983
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 29.