BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 30939887)

  • 1. Noonan syndrome from a fetopathologist perspective.
    Stupková T; Ježová M; Matyášová M; Vlašín P
    Cesk Patol; 2019; 55(1):48-52. PubMed ID: 30939887
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis of Noonan syndrome in fetuses with increased nuchal translucency and a normal karyotype.
    Matyášová M; Dobšáková Z; Hiemerová M; Kadlecová J; Nikulenkov Grochová D; Popelínská E; Svobodová E; Vlašín P
    Ceska Gynekol; 2019; 84(3):195-200. PubMed ID: 31324109
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Targeted ultrasound examination and DNA testing for Noonan syndrome, in fetuses with increased nuchal translucency and normal karyotype.
    Bakker M; Pajkrt E; Mathijssen IB; Bilardo CM
    Prenat Diagn; 2011 Sep; 31(9):833-40. PubMed ID: 21706501
    [TBL] [Abstract][Full Text] [Related]  

  • 4. First trimester cystic hygroma colli: Retrospective analysis in a tertiary center.
    Schreurs L; Lannoo L; De Catte L; Van Schoubroeck D; Devriendt K; Richter J
    Eur J Obstet Gynecol Reprod Biol; 2018 Dec; 231():60-64. PubMed ID: 30321790
    [TBL] [Abstract][Full Text] [Related]  

  • 5. PTPN11 analysis for the prenatal diagnosis of Noonan syndrome in fetuses with abnormal ultrasound findings.
    Lee KA; Williams B; Roza K; Ferguson H; David K; Eddleman K; Stone J; Edelmann L; Richard G; Gelb BD; Kornreich R
    Clin Genet; 2009 Feb; 75(2):190-4. PubMed ID: 18759865
    [TBL] [Abstract][Full Text] [Related]  

  • 6. How necessary is to analyze PTPN11 gene in fetuses with first trimester cystic hygroma and normal karyotype?
    Gezdirici A; Ekiz A; Güleç EY; Kaya B; Sezer S; Atış Aydın A
    J Matern Fetal Neonatal Med; 2017 Apr; 30(8):938-941. PubMed ID: 27193571
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Karyotype and outcome of fetuses diagnosed with cystic hygroma in the first trimester in relation to nuchal translucency thickness.
    Kharrat R; Yamamoto M; Roume J; Couderc S; Vialard F; Hillion Y; Ville Y
    Prenat Diagn; 2006 Apr; 26(4):369-72. PubMed ID: 16566042
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Fetal Phenotype of Noonan Syndrome Caused by Severe, Cancer-Related PTPN11 Variants.
    Malniece I; Grasmane A; Inashkina I; Stavusis J; Kreile M; Miklasevics E; Gailite L
    Am J Case Rep; 2020 Jul; 21():e922468. PubMed ID: 32794475
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Increased nuchal translucency and cystic hygroma in the first trimester: prenatal diagnosis and neonatal outcome].
    Ducarme G; Graesslin O; Alanio E; Bige V; Gaillard D; Gabriel R
    Gynecol Obstet Fertil; 2005 Oct; 33(10):750-4. PubMed ID: 16139544
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings.
    Croonen EA; Nillesen WM; Stuurman KE; Oudesluijs G; van de Laar IM; Martens L; Ockeloen C; Mathijssen IB; Schepens M; Ruiterkamp-Versteeg M; Scheffer H; Faas BH; van der Burgt I; Yntema HG
    Eur J Hum Genet; 2013 Sep; 21(9):936-42. PubMed ID: 23321623
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Persistence of nuchal edema and distended jugular lymphatic sacs in Noonan syndrome.
    Bekker MN; Go AT; van Vugt JM
    Fetal Diagn Ther; 2007; 22(4):245-8. PubMed ID: 17369688
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal ultrasound findings of rasopathies in a cohort of 424 fetuses: update on genetic testing in the NGS era.
    Stuurman KE; Joosten M; van der Burgt I; Elting M; Yntema HG; Meijers-Heijboer H; Rinne T
    J Med Genet; 2019 Oct; 56(10):654-661. PubMed ID: 31040167
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Distended jugular lymphatic sacs in fetuses with increased nuchal translucency: correlation with first-trimester findings in aberrant karyotypes.
    Eckmann-Scholz C; Salmassi A; Jonat W; Alkatout I
    J Matern Fetal Neonatal Med; 2014 Feb; 27(3):257-60. PubMed ID: 23718767
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multiple marker screening test: identification of fetal cystic hygroma, hydrops, and sex chromosome aneuploidy.
    Wenstrom KD; Boots LR; Cosper PC
    J Matern Fetal Med; 1996; 5(1):31-5. PubMed ID: 8796763
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Three fetuses karyotyped as Turner syndrome with cystic hygroma developing hydrops: prognosis and outcome.
    Basgul A; Güdücü N; Kavak ZN; Gökaslan H; Uyar E
    Clin Exp Obstet Gynecol; 2007; 34(3):182-4. PubMed ID: 17937097
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal features of Noonan syndrome.
    Nisbet DL; Griffin DR; Chitty LS
    Prenat Diagn; 1999 Jul; 19(7):642-7. PubMed ID: 10419612
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Postnatal phenotype according to prenatal ultrasound features of Noonan syndrome: a retrospective study of 28 cases.
    Gaudineau A; Doray B; Schaefer E; Sananès N; Fritz G; Kohler M; Alembik Y; Viville B; Favre R; Langer B
    Prenat Diagn; 2013 Mar; 33(3):238-41. PubMed ID: 23345196
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Analysis for the pregnancy outcome of cystic hygroma fetuses and correlation with increased nuchal translucency in first trimester].
    Wang Q; Wang X
    Zhonghua Fu Chan Ke Za Zhi; 2018 Oct; 53(10):665-670. PubMed ID: 30369121
    [No Abstract]   [Full Text] [Related]  

  • 19. Aberrant lymphatic development in euploid fetuses with increased nuchal translucency including Noonan syndrome.
    de Mooij YM; van den Akker NM; Bekker MN; Bartelings MM; van Vugt JM; Gittenberger-de Groot AC
    Prenat Diagn; 2011 Feb; 31(2):159-66. PubMed ID: 21268034
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A case report of Turner syndrome associated with fetal nuchal cystic hygroma and bilateral syndactyly of the hands and feet.
    Chen HY; Zheng JQ; Zhang HP
    Ital J Pediatr; 2019 Jul; 45(1):85. PubMed ID: 31319890
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.