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Journal Abstract Search

189 related items for PubMed ID: 24357154

  • 21. Fryns syndrome: a review of the phenotype and diagnostic guidelines.
    Slavotinek AM.
    Am J Med Genet A; 2004 Feb 01; 124A(4):427-33. PubMed ID: 14735597
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  • 24. Fryns syndrome with vertebral defects: a novel association in a Mexican infant.
    Salinas-Torres VM, Rivera H.
    Genet Couns; 2014 Feb 01; 25(1):29-33. PubMed ID: 24783652
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  • 25. Schinzel-Giedion syndrome: a novel case, review and revised diagnostic criteria.
    Liu WL, He ZX, Li F, Ai R, Ma HW.
    J Genet; 2018 Mar 01; 97(1):35-46. PubMed ID: 29666323
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  • 26. A case of Fryns syndrome without diaphragmatic hernia and review of the literature.
    Vasudevan PC, Stewart H.
    Clin Dysmorphol; 2004 Jul 01; 13(3):179-182. PubMed ID: 15194956
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  • 27. Phenotype-genotype complexities: opening DOORS.
    Berkovic SF, Gecz J.
    Lancet Neurol; 2014 Jan 01; 13(1):24-5. PubMed ID: 24291219
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  • 28. Kaufman oculo-cerebro-facial syndrome in a child with small and absent terminal phalanges and absent nails.
    Kariminejad A, Ajeawung NF, Bozorgmehr B, Dionne-Laporte A, Molidperee S, Najafi K, Gibbs RA, Lee BH, Hennekam RC, Campeau PM.
    J Hum Genet; 2017 Apr 01; 62(4):465-471. PubMed ID: 28003643
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  • 29. Atypical Fryns syndrome: clinical, radiological and pathological findings.
    Aygün MS, Sekmenli T, Çiftçi İ, Gökmen Z, Tolu İ, Mutlu-Aygün F.
    Turk J Pediatr; 2014 Apr 01; 56(1):107-10. PubMed ID: 24827959
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  • 30. DOORS syndrome: phenotype, genotype and comparison with Coffin-Siris syndrome.
    Campeau PM, Hennekam RC, DOORS syndrome collaborative group.
    Am J Med Genet C Semin Med Genet; 2014 Sep 01; 166C(3):327-32. PubMed ID: 25169651
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  • 33. Fryns syndrome: two further cases without lateral diaphragmatic defects.
    Bartsch O, Meinecke P, Kamin G.
    Clin Dysmorphol; 1995 Oct 01; 4(4):352-8. PubMed ID: 8574427
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  • 35. Fryns syndrome: case report and review of the literature.
    Yucesoy G, Cakiroglu Y, Caliskan E.
    J Clin Ultrasound; 2008 Jun 01; 36(5):315-7. PubMed ID: 17960800
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  • 36. Fryns syndrome phenotype and trisomy 22.
    Ladonne JM, Gaillard D, Carré-Pigeon F, Gabriel R.
    Am J Med Genet; 1996 Jan 02; 61(1):68-70. PubMed ID: 8741922
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  • 39. West syndrome in a patient with Schinzel-Giedion syndrome.
    Miyake F, Kuroda Y, Naruto T, Ohashi I, Takano K, Kurosawa K.
    J Child Neurol; 2015 Jun 02; 30(7):932-6. PubMed ID: 25028416
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