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Journal Abstract Search

130 related items for PubMed ID: 11223711

  • 1. Antenatal three-dimensional sonographic features of Pierre-Robin syndrome. Case report.
    Matsumoto M, Yanagihara T, Hanaoka U, Maesato T, Kuno A, Yamashiro C, Tanaka H, Hayashi K, Hata T.
    Gynecol Obstet Invest; 2001; 51(2):141-2. PubMed ID: 11223711
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  • 2. The prenatal diagnosis of Pierre-Robin sequence.
    Hsieh YY, Chang CC, Tsai HD, Yang TC, Lee CC, Tsai CH.
    Prenat Diagn; 1999 Jun; 19(6):567-9. PubMed ID: 10416975
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  • 3. Ultrasonographic diagnosis of glossoptosis in fetuses with Pierre Robin sequence in early and mid pregnancy.
    Bronshtein M, Blazer S, Zalel Y, Zimmer EZ.
    Am J Obstet Gynecol; 2005 Oct; 193(4):1561-4. PubMed ID: 16202757
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  • 4. First-trimester diagnosis of micrognathia as a presentation of Pierre Robin syndrome.
    Teoh M, Meagher S.
    Ultrasound Obstet Gynecol; 2003 Jun; 21(6):616-8. PubMed ID: 12808682
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  • 5. Prenatal Identification of Pierre Robin Sequence: A Review of the Literature and Look towards the Future.
    Kaufman MG, Cassady CI, Hyman CH, Lee W, Watcha MF, Hippard HK, Olutoye OA, Khechoyan DY, Monson LA, Buchanan EP.
    Fetal Diagn Ther; 2016 Jun; 39(2):81-9. PubMed ID: 25967128
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  • 10. Prenatal diagnosis of Pierre-Robin sequence as part of Stickler syndrome.
    Soulier M, Sigaudy S, Chau C, Philip N.
    Prenat Diagn; 2002 Jul; 22(7):567-8. PubMed ID: 12124689
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  • 11. Syndromic micrognathia and peri-natal management with the ex-utero intra-partum treatment (EXIT) procedure.
    Costello BJ, Hueser T, Mandell D, Hackam D, Prosen TL.
    Int J Oral Maxillofac Surg; 2010 Jul; 39(7):725-8. PubMed ID: 20303239
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  • 13. The prenatal diagnosis of Robin anomalad.
    Pilu G, Romero R, Reece EA, Jeanty P, Hobbins JC.
    Am J Obstet Gynecol; 1986 Mar; 154(3):630-2. PubMed ID: 3513591
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  • 14. Prenatal diagnosis of Pierre Robin Sequence: accuracy and ability to predict phenotype and functional severity.
    Lind K, Aubry MC, Belarbi N, Chalouhi C, Couly G, Benachi A, Lyonnet S, Abadie V.
    Prenat Diagn; 2015 Sep; 35(9):853-8. PubMed ID: 25982360
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  • 15. Fetal manifestation of the Fine-Lubinsky syndrome. Brachycephaly, deafness, cataract, microstomia and mental retardation syndrome complicated by Pierre-Robin anomaly and polyhydramnios.
    Schoner K, Bald R, Fritz B, Rehder H.
    Fetal Diagn Ther; 2008 Sep; 23(3):228-32. PubMed ID: 18417983
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  • 16. Prenatal ultrasound detection of micrognathia and its association with Robin sequence.
    Kimakhe J, Gilleard O, Swan MC, Pandya P, Thakur V, Ushakov F, Regan L, Minhas M, Bailey J, Hughes J, Codling P, Morris P, Thorburn G, Lees M, McEvoy M, Abel F, Cochrane L, Harding L, Nambiar S, Chorbachi R, Seselgyte R, Hay N, Patel B, Kangesu L.
    J Plast Reconstr Aesthet Surg; 2017 Sep; 70(9):1308-1311. PubMed ID: 28734755
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  • 17. An objective measurement to diagnose micrognathia on prenatal ultrasound.
    Palit G, Jacquemyn Y, Kerremans M.
    Clin Exp Obstet Gynecol; 2008 Sep; 35(2):121-3. PubMed ID: 18581766
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  • 18. Prenatal diagnosis of femoral-facial syndrome: report of two cases.
    Silvas E, Rypens F, Jovanovic M, Delezoide AL, Patey N.
    Birth Defects Res A Clin Mol Teratol; 2013 Dec; 97(12):770-3. PubMed ID: 24254654
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  • 19. Efficiency of prenatal diagnosis in Pierre Robin sequence.
    Di Pasquo E, Amiel J, Roth P, Malan V, Lind K, Chalouhi C, Soupre V, Gordon CT, Lyonnet S, Salomon LJ, Abadie V.
    Prenat Diagn; 2017 Nov; 37(11):1169-1175. PubMed ID: 28950416
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  • 20. Twins with Pierre Robin syndrome.
    Pruzansky S.
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):72-5. PubMed ID: 5173778
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