BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

219 related articles for article (PubMed ID: 16032767)

  • 1. Prenatal DNA diagnosis of Noonan syndrome in a fetus with massive hygroma colli, pleural effusion and ascites.
    Schlüter G; Steckel M; Schiffmann H; Harms K; Viereck V; Emons G; Burfeind P; Pauer HU
    Prenat Diagn; 2005 Jul; 25(7):574-6. PubMed ID: 16032767
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 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. 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]  

  • 5. 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]  

  • 6. Prenatal sonographic documentation of cystic hygroma regression in Noonan syndrome.
    Donnenfeld AE; Nazir MA; Sindoni F; Librizzi RJ
    Am J Med Genet; 1991 Jun; 39(4):461-5. PubMed ID: 1877625
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Severe aortic valvar stenosis in familial Noonan syndrome with mutation of the PTPN11 gene.
    Abadir S; Edouard T; Julia S
    Cardiol Young; 2007 Feb; 17(1):95-7. PubMed ID: 17184563
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Noonan syndrome.
    van der Burgt I
    Orphanet J Rare Dis; 2007 Jan; 2():4. PubMed ID: 17222357
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Noonan-like syndrome mutations in PTPN11 in patients diagnosed with cherubism.
    Jafarov T; Ferimazova N; Reichenberger E
    Clin Genet; 2005 Aug; 68(2):190-1. PubMed ID: 15996221
    [No Abstract]   [Full Text] [Related]  

  • 10. PTPN11 gene analysis in 74 Brazilian patients with Noonan syndrome or Noonan-like phenotype.
    Bertola DR; Pereira AC; Albano LM; De Oliveira PS; Kim CA; Krieger JE
    Genet Test; 2006; 10(3):186-91. PubMed ID: 17020470
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Spontaneous resolution of cystic hygroma and hydrops in a fetus with Noonan's syndrome.
    Kiyota A; Tsukimori K; Yumoto Y; Hojo S; Morokuma S; Fukushima K; Takahata Y; Nakayama H; Wake N
    Fetal Diagn Ther; 2008; 24(4):499-502. PubMed ID: 19151555
    [TBL] [Abstract][Full Text] [Related]  

  • 13. PTPN11 gene mutations: linking the Gln510Glu mutation to the "LEOPARD syndrome phenotype".
    Digilio MC; Sarkozy A; Pacileo G; Limongelli G; Marino B; Dallapiccola B
    Eur J Pediatr; 2006 Nov; 165(11):803-5. PubMed ID: 16733669
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Noonan syndrome: prenatal diagnosis in a woman carrying a PTPN11 gene mutation.
    González-Huerta NC; Valdés-Miranda JM; Pérez-Cabrera A; Pacheco-Cuellar G; González-Huerta LM; Cuevas-Covarrubias SA
    J Matern Fetal Neonatal Med; 2010 Jul; 23(7):688-91. PubMed ID: 20064076
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Third trimester resolution of cystic hygroma and pleural effusion in a fetus with Turner syndrome.
    Brookhyser KM; Slotnick RN; Hanson FW
    Am J Perinatol; 1993 Jul; 10(4):297-9. PubMed ID: 8397566
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fetal therapy and cytogenetic testing: prenatal detection of chromosome aberration during thoracocentesis for congenital chylothorax by karyotyping from pleural effusion fluid and review of the literature.
    Chen CP
    Genet Couns; 2005; 16(3):301-5. PubMed ID: 16259328
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The spectrum of cardiac anomalies in Noonan syndrome as a result of mutations in the PTPN11 gene.
    Sznajer Y; Keren B; Baumann C; Pereira S; Alberti C; Elion J; Cavé H; Verloes A
    Pediatrics; 2007 Jun; 119(6):e1325-31. PubMed ID: 17515436
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.