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Journal Abstract Search

234 related items for PubMed ID: 16396829

  • 1. Prenatal death in Fraser syndrome.
    Comstock JM, Putnam AR, Opitz JM, Pysher TJ, Szakacs J.
    Fetal Pediatr Pathol; 2005; 24(4-5):223-38. PubMed ID: 16396829
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  • 3. 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; 11(3):220-5. PubMed ID: 17990920
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  • 5. Fraser syndrome: a new case report with review of the literature.
    Eskander BS, Shehata BM.
    Fetal Pediatr Pathol; 2008; 27(2):99-104. PubMed ID: 18568997
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  • 8. 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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  • 9. Fraser syndrome: recurrence in a family.
    Singh R, Tandon I, Deo S.
    Indian Pediatr; 2007 Dec; 44(12):929-30. PubMed ID: 18175849
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  • 11. Fraser (Cryptophthalmos-syndactyly) syndrome: a case with bilateral anophthalmia but presence of normal eyelids.
    Pankau R, Partsch CJ, Jänig U, Meinecke R.
    Genet Couns; 1994 Dec; 5(2):191-4. PubMed ID: 7917132
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  • 12. 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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  • 13. Fraser syndrome. Cryptophthalmos syndactyly syndrome.
    Tilahun M, Kifle A, Oljira B.
    Ethiop Med J; 1990 Apr; 28(2):89-90. PubMed ID: 2163830
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  • 14. Fraser Syndrome.
    Saleem AA, Siddiqui SN.
    J Coll Physicians Surg Pak; 2015 Oct; 25 Suppl 2():S124-6. PubMed ID: 26522198
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  • 18. Fraser syndrome.
    Kalpana Kumari MK, Kamath S, Mysorekar VV, Nandini G.
    Indian J Pathol Microbiol; 2008 Oct; 51(2):228-9. PubMed ID: 18603689
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  • 19. Fraser syndrome (cryptophthalmos-syndactyly syndrome): a review of eleven cases with postmortem findings.
    Boyd PA, Keeling JW, Lindenbaum RH.
    Am J Med Genet; 1988 Sep; 31(1):159-68. PubMed ID: 2851937
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  • 20. Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein.
    McGregor L, Makela V, Darling SM, Vrontou S, Chalepakis G, Roberts C, Smart N, Rutland P, Prescott N, Hopkins J, Bentley E, Shaw A, Roberts E, Mueller R, Jadeja S, Philip N, Nelson J, Francannet C, Perez-Aytes A, Megarbane A, Kerr B, Wainwright B, Woolf AS, Winter RM, Scambler PJ.
    Nat Genet; 2003 Jun; 34(2):203-8. PubMed ID: 12766769
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