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 *

150 related articles for article (PubMed ID: 33939854)

  • 1. New genetic and clinical evidence associated with fetal Beckwith-Wiedemann syndrome.
    Traisrisilp K; Chankhunaphas W; Sirilert S; Kuwutiyakorn V; Tongsong T
    Prenat Diagn; 2021 Jun; 41(7):823-827. PubMed ID: 33939854
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial Beckwith-Wiedemann syndrome: Prenatal manifestation and a possible expansion of the phenotype.
    Brabbing-Goldstein D; Yaron Y; Reches A
    Eur J Med Genet; 2021 Feb; 64(2):104137. PubMed ID: 33421606
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Beckwith-Wiedemann Syndrome in Newborn of Mother with HELLP Syndrome/Preeclampsia: An Analysis of Literature and Case Report with Fetal Growth Restriction and Absence of
    Staniczek J; Manasar-Dyrbuś M; Drosdzol-Cop A; Stojko R
    Int J Mol Sci; 2023 Aug; 24(17):. PubMed ID: 37686168
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Beckwith-Wiedemann syndrome: What do you search in prenatal diagnosis? About 14 cases].
    Le Vaillant C; Beneteau C; Chan-Leconte N; David A; Riteau AS
    Gynecol Obstet Fertil; 2015 Nov; 43(11):705-11. PubMed ID: 26542939
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis of the Beckwith-Wiedemann syndrome.
    Winter SC; Curry CJ; Smith JC; Kassel S; Miller L; Andrea J
    Am J Med Genet; 1986 May; 24(1):137-41. PubMed ID: 3518454
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fetal Beckwith-Wiedemann syndrome associated with abnormal quad test, placental mesenchymal dysplasia and HELLP syndrome.
    Jatavan P; Tongsong T; Traisrisilp K
    BMJ Case Rep; 2021 Jun; 14(6):. PubMed ID: 34167990
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fetal intracardiac rhabdomyoma in beckwith-wiedemann syndrome.
    Longardt AC; Nonnenmacher A; Graul-Neumann L; Opgen-Rhein B; Henrich W; Bührer C; Hüseman D
    J Clin Ultrasound; 2014; 42(9):569-73. PubMed ID: 24752985
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal imaging throughout gestation in Beckwith-Wiedemann syndrome.
    Shieh HF; Estroff JA; Barnewolt CE; Zurakowski D; Tan WH; Buchmiller TL
    Prenat Diagn; 2019 Aug; 39(9):792-795. PubMed ID: 30784096
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel fetal and maternal sonographic findings in confirmed cases of Beckwith-Wiedemann syndrome.
    Kagan KO; Berg C; Dufke A; Geipel A; Hoopmann M; Abele H
    Prenat Diagn; 2015 Apr; 35(4):394-9. PubMed ID: 25641174
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Wiedemann-Beckwith syndrome: further prenatal characterization of the condition.
    Reish O; Lerer I; Amiel A; Heyman E; Herman A; Dolfin T; Abeliovich D
    Am J Med Genet; 2002 Jan; 107(3):209-13. PubMed ID: 11807901
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Isolated fetal omphalocele, Beckwith-Wiedemann syndrome, and assisted reproductive technologies.
    Wilkins-Haug L; Porter A; Hawley P; Benson CB
    Birth Defects Res A Clin Mol Teratol; 2009 Jan; 85(1):58-62. PubMed ID: 19107956
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Kagami-Ogata syndrome: an important differential diagnosis to Beckwith-Wiedemann syndrome.
    Altmann J; Horn D; Korinth D; Eggermann T; Henrich W; Verlohren S
    J Clin Ultrasound; 2020 May; 48(4):240-243. PubMed ID: 31994200
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis in autosomal dominant Beckwith-Wiedemann syndrome.
    Viljoen DL; Jaquire Z; Woods DL
    Prenat Diagn; 1991 Mar; 11(3):167-75. PubMed ID: 2038600
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Syndromes and disorders associated with omphalocele (I): Beckwith-Wiedemann syndrome.
    Chen CP
    Taiwan J Obstet Gynecol; 2007 Jun; 46(2):96-102. PubMed ID: 17638616
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CDKN1C (p57(Kip2)) analysis in Beckwith-Wiedemann syndrome (BWS) patients: Genotype-phenotype correlations, novel mutations, and polymorphisms.
    Romanelli V; Belinchón A; Benito-Sanz S; Martínez-Glez V; Gracia-Bouthelier R; Heath KE; Campos-Barros A; García-Miñaur S; Fernandez L; Meneses H; López-Siguero JP; Guillén-Navarro E; Gómez-Puertas P; Wesselink JJ; Mercado G; Esteban-Marfil V; Palomo R; Mena R; Sánchez A; Del Campo M; Lapunzina P
    Am J Med Genet A; 2010 Jun; 152A(6):1390-7. PubMed ID: 20503313
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Elevated maternal serum α-fetoprotein level in a fetus with Beckwith-Wiedemann syndrome in the second trimester of pregnancy.
    Guanciali-Franchi P; Di Luzio L; Iezzi I; Celentano C; Matarrelli B; Liberati M; Palka G
    J Prenat Med; 2012 Jan; 6(1):7-9. PubMed ID: 22905304
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Overrepresentation of pregnancies conceived by artificial reproductive technology in prenatally identified fetuses with Beckwith-Wiedemann syndrome.
    Johnson JP; Beischel L; Schwanke C; Styren K; Crunk A; Schoof J; Elias AF
    J Assist Reprod Genet; 2018 Jun; 35(6):985-992. PubMed ID: 29936652
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.
    Calvello M; Tabano S; Colapietro P; Maitz S; Pansa A; Augello C; Lalatta F; Gentilin B; Spreafico F; Calzari L; Perotti D; Larizza L; Russo S; Selicorni A; Sirchia SM; Miozzo M
    Epigenetics; 2013 Oct; 8(10):1053-60. PubMed ID: 23917791
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal sonographic diagnosis of Beckwith-Wiedemann syndrome in association with a single umbilical artery.
    Hamada H; Fujiki Y; Obata-Yasuoka M; Watanabe H; Yamada N; Kubo T
    J Clin Ultrasound; 2001; 29(9):535-8. PubMed ID: 11745867
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation.
    Lam WW; Hatada I; Ohishi S; Mukai T; Joyce JA; Cole TR; Donnai D; Reik W; Schofield PN; Maher ER
    J Med Genet; 1999 Jul; 36(7):518-23. PubMed ID: 10424811
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.