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Journal Abstract Search

105 related items for PubMed ID: 3482048

  • 1.
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  • 2. [Saethre-Chötzen syndrome. A study apropos of 17 cases].
    Ferri J, Seiler C, Piot B, Mercier J.
    Rev Stomatol Chir Maxillofac; 1993; 94(5):290-9. PubMed ID: 8235424
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  • 3. [Morphological evaluation on craniofacial dysmorphology of Apert's syndrome and Crouzon disease].
    Susami T, Terashima T, Lin TZ, Motohashi N, Kuroda T.
    Nihon Kyosei Shika Gakkai Zasshi; 1986 Dec; 45(4):674-86. PubMed ID: 3505581
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  • 8. 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. Facial variability in Apert type acrocephalosyndactyly.
    Cohen MM, Gorlin RJ, Berkman MD, Feingold M.
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):143-6. PubMed ID: 5173202
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  • 13. Apert syndrome.
    PremalathaDepartment of Pedodontics, GDC, Calicut, India. speakprema@ymail.com, Kannan VP, Madhu.
    J Indian Soc Pedod Prev Dent; 2010 Jun; 28(4):322-5. PubMed ID: 21273726
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  • 14. Cranial size and configuration in the Apert syndrome.
    Cohen MM, Kreiborg S.
    J Craniofac Genet Dev Biol; 1994 Jun; 14(3):153-62. PubMed ID: 7852544
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  • 15. Pfeiffer syndrome or Saethre-Chotzen syndrome?
    Tsukahara M, Hagiwara K, Kajii T.
    Jinrui Idengaku Zasshi; 1985 Jun; 30(2):51-6. PubMed ID: 4087491
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  • 16. Picture of the month. Acrocephalosyndactyly type Saethre-Chotzen (Saethre-Chotzen syndrome).
    Gellis SS, Feingold M.
    Am J Dis Child; 1975 Feb; 129(2):227-8. PubMed ID: 1119458
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  • 17. [Familial acrocephalosyndactylia with features of the Saethre-Chotzen syndrome].
    Kopyść Z, Kulczyk B, Ryzko J, Gura C, Stańska M, Kowalski K.
    Pediatr Pol; 1979 Jul; 54(7):769-72. PubMed ID: 530768
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  • 18. 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 Jul; 56(2):195-204. PubMed ID: 7450776
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  • 19. Saethre-Chotzen syndrome with familial translocation at chromosome 7p22.
    Reid CS, McMorrow LE, McDonald-McGinn DM, Grace KJ, Ramos FJ, Zackai EH, Cohen MM, Jabs EW.
    Am J Med Genet; 1993 Oct 01; 47(5):637-9. PubMed ID: 8266989
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  • 20. Cephalometric study of the Apert syndrome in adolescence and adulthood.
    Kreiborg S, Aduss H, Cohen MM.
    J Craniofac Genet Dev Biol; 1999 Oct 01; 19(1):1-11. PubMed ID: 10378142
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