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Journal Abstract Search

166 related items for PubMed ID: 10817648

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  • 2. 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
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  • 3. Persistently elevated nuchal translucency and the fetal heart.
    Vigneswaran TV, Homfray T, Allan LD, Simpson JM, Zidere V.
    J Matern Fetal Neonatal Med; 2018 Sep; 31(18):2376-2380. PubMed ID: 28614966
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  • 6. Persistence of nuchal edema and distended jugular lymphatic sacs in Noonan syndrome.
    Bekker MN, Go AT, van Vugt JM.
    Fetal Diagn Ther; 2007 Sep; 22(4):245-8. PubMed ID: 17369688
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  • 7. Poor prenatal detection rate of cardiac anomalies in Noonan syndrome.
    Menashe M, Arbel R, Raveh D, Achiron R, Yagel S.
    Ultrasound Obstet Gynecol; 2002 Jan; 19(1):51-5. PubMed ID: 11851968
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  • 8. 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
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  • 9. Prenatal phenotypic overlap of Costello syndrome and severe Noonan syndrome by tri-dimensional ultrasonography.
    Levaillant JM, Gérard-Blanluet M, Holder-Espinasse M, Valat-Rigot AS, Devisme L, Cavé H, Manouvrier-Hanu S.
    Prenat Diagn; 2006 Apr; 26(4):340-4. PubMed ID: 16566035
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  • 10. 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
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  • 14. 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
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  • 15. Noonan syndrome from a fetopathologist perspective.
    Stupková T, Ježová M, Matyášová M, Vlašín P.
    Cesk Patol; 2019 Jul; 55(1):48-52. PubMed ID: 30939887
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  • 16. 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 31; 21():e922468. PubMed ID: 32794475
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  • 17. Increased nuchal translucency as a marker for fetal chromosomal defects.
    Taipale P, Hiilesmaa V, Salonen R, Ylöstalo P.
    N Engl J Med; 1997 Dec 04; 337(23):1654-8. PubMed ID: 9385124
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  • 18. 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 04; 21(9):936-42. PubMed ID: 23321623
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  • 19. A Novel Mutation on RAF1 in Association with Fetal Findings Suggestive of Noonan Syndrome.
    Kneitel AW, Norby A, Vettraino I, Treadwell MC.
    Fetal Pediatr Pathol; 2015 Sep 04; 34(6):361-4. PubMed ID: 26467173
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  • 20. 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 04; 231():60-64. PubMed ID: 30321790
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