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PUBMED FOR HANDHELDS

Journal Abstract Search


142 related items for PubMed ID: 7793794

  • 1. Familial Saethre-Chotzen syndrome with or without polydactyly of the toe.
    Shidayama R, Hirano A, Iio Y, Fujii T.
    Ann Plast Surg; 1995 Apr; 34(4):435-40. PubMed ID: 7793794
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  • 2. The Saethre-Chotzen syndrome with partial bifid of the distal phalanges of the great toes. Observations of three cases in one family.
    Kopyść Z, Stańska M, Ryzko J, Kulczyk B.
    Hum Genet; 1980 Apr; 56(2):195-204. PubMed ID: 7450776
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  • 3. Saethre-Chotzen syndrome: a broad and variable pattern of skeletal malformations.
    Friedman JM, Hanson JW, Graham CB, Smith DW.
    J Pediatr; 1977 Dec; 91(6):929-23. PubMed ID: 925822
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  • 5. A novel mutation in the TWIST gene, implicated in Saethre-Chotzen syndrome, is found in the original case of Robinow-Sorauf syndrome.
    Cai J, Shoo BA, Sorauf T, Jabs EW.
    Clin Genet; 2003 Jul; 64(1):79-82. PubMed ID: 12791045
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  • 9. A family with the Saethre-Chotzen syndrome.
    Bianchi E, Aricŏ M, Podestă AF, Grana M, Fiori P, Beluffi G.
    Am J Med Genet; 1985 Dec; 22(4):649-58. PubMed ID: 4073118
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  • 11. Cephalic malformations in Saethre-Chotzen syndrome. Acrocephalosyndactyly type III.
    Evans CA, Christiansen RL.
    Radiology; 1976 Nov; 121(2):399-403. PubMed ID: 981618
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  • 12. Identification of a frameshift mutation in the gene TWIST in a family affected with Robinow-Sorauf syndrome.
    Kunz J, Hudler M, Fritz B.
    J Med Genet; 1999 Aug; 36(8):650-2. PubMed ID: 10465122
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  • 13. A novel frameshift mutation of the GLI3 gene in a family with broad thumbs with/without big toes, postaxial polydactyly and variable syndactyly of the hands/feet.
    Al-Qattan MM.
    Clin Genet; 2012 Nov; 82(5):502-4. PubMed ID: 22428873
    [No Abstract] [Full Text] [Related]

  • 14. Morphology of the foramen magnum in syndromic and non-syndromic brachycephaly.
    Assadsangabi R, Hajmomenian M, Bilaniuk LT, Vossough A.
    Childs Nerv Syst; 2015 May; 31(5):735-41. PubMed ID: 25686894
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  • 15. A child with Saethre-Chotzen syndrome, sensorineural hearing loss, and a TWIST mutation.
    Lee S, Seto M, Sie K, Cunningham M.
    Cleft Palate Craniofac J; 2002 Jan; 39(1):110-4. PubMed ID: 11772178
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  • 16. Atypical crossed polydactyly in two siblings with Ellis-van Creveld Syndrome and mild clinical manifestations in close relatives.
    Okten A, Cakir M, Orhan F, Mungan I.
    Pediatr Int; 2004 Apr; 46(2):184-7. PubMed ID: 15056248
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  • 17. The Saethre-Chotzen syndrome.
    Kreiborg S, Pruzansky S, Pashayan H.
    Teratology; 1972 Dec; 6(3):287-94. PubMed ID: 4643612
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  • 18. Saethre-Chotzen syndrome (ACS III) in four generations.
    Niemann-Seyde SC, Eber SW, Zoll B.
    Clin Genet; 1991 Oct; 40(4):271-6. PubMed ID: 1756600
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  • 19. Craniofacial morphology and growth in Muenke syndrome, Saethre-Chotzen syndrome, and TCF12-related craniosynostosis.
    Choi TM, Lijten OW, Mathijssen IMJ, Wolvius EB, Ongkosuwito EM.
    Clin Oral Investig; 2022 Mar; 26(3):2927-2936. PubMed ID: 34904178
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  • 20. Foot polydactyly and polysyndactyly: genetic implications in two families.
    Hwang K, Kim ET, Lee SI.
    J Foot Ankle Surg; 2005 Mar; 44(6):473-7. PubMed ID: 16257679
    [Abstract] [Full Text] [Related]


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