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Journal Abstract Search

193 related items for PubMed ID: 26522198

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  • 2. Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes.
    Slavotinek AM, Tifft CJ.
    J Med Genet; 2002 Sep; 39(9):623-33. PubMed ID: 12205104
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  • 4. Fraser syndrome: affected siblings born to nonconsanguineous parents and diagnosed at autopsy.
    De Jong A, Warren M, Rehrauer W, Harter J, Baraboo M, Chandra S, Pauli RM, Singer DB, Fritsch MK.
    Pediatr Dev Pathol; 2008 Sep; 11(3):220-5. PubMed ID: 17990920
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  • 6. Fraser syndrome: review of the literature illustrated by a historical adult case.
    Bouaoud J, Olivetto M, Testelin S, Dakpe S, Bettoni J, Devauchelle B.
    Int J Oral Maxillofac Surg; 2020 Oct; 49(10):1245-1253. PubMed ID: 31982235
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  • 9. Prenatal diagnosis of Fraser syndrome: a matter of life or death?
    De Bernardo G, Giordano M, Di Toro A, Sordino D, De Brasi D.
    Ital J Pediatr; 2015 Nov 09; 41():86. PubMed ID: 26552811
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  • 10. Molecular study of 33 families with Fraser syndrome new data and mutation review.
    van Haelst MM, Maiburg M, Baujat G, Jadeja S, Monti E, Bland E, Pearce K, Fraser Syndrome Collaboration Group, Hennekam RC, Scambler PJ.
    Am J Med Genet A; 2008 Sep 01; 146A(17):2252-7. PubMed ID: 18671281
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  • 11. Prenatal diagnosis of Fraser syndrome at 18.5 weeks gestation, with autopsy findings at 19 weeks.
    Schauer GM, Dunn LK, Godmilow L, Eagle RC, Knisely AS.
    Am J Med Genet; 1990 Dec 01; 37(4):583-91. PubMed ID: 2175543
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  • 13. Prenatal death in Fraser syndrome.
    Comstock JM, Putnam AR, Opitz JM, Pysher TJ, Szakacs J.
    Fetal Pediatr Pathol; 2005 Dec 01; 24(4-5):223-38. PubMed ID: 16396829
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  • 14. Prenatal detection of Fraser syndrome without cryptophthalmos: case report and review of the literature.
    Berg C, Geipel A, Germer U, Pertersen-Hansen A, Koch-Dörfler M, Gembruch U.
    Ultrasound Obstet Gynecol; 2001 Jul 01; 18(1):76-80. PubMed ID: 11489232
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  • 15. Fraser syndrome without cryptophthalmos: Two cases.
    Boussion S, Lyonnet S, Van Der Zwaag B, Vogel MJ, Smol T, Mezel A, Manouvrier-Hanu S, Vincent-Delorme C, Vanlerberghe C.
    Eur J Med Genet; 2020 Apr 01; 63(4):103839. PubMed ID: 31923588
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  • 19. Mutations in GRIP1 cause Fraser syndrome.
    Vogel MJ, van Zon P, Brueton L, Gijzen M, van Tuil MC, Cox P, Schanze D, Kariminejad A, Ghaderi-Sohi S, Blair E, Zenker M, Scambler PJ, Ploos van Amstel HK, van Haelst MM.
    J Med Genet; 2012 May 01; 49(5):303-6. PubMed ID: 22510445
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