155 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]
