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Journal Abstract Search

213 related items for PubMed ID: 1227525

  • 1.
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  • 2. An etiologic and nosologic overview of craniosynostosis syndromes.
    Cohen MM.
    Birth Defects Orig Artic Ser; 1975; 11(2):137-89. PubMed ID: 179637
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  • 4. 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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  • 6. Auralcephalosyndactyly: a new craniosynostosis syndrome or a variant of the Saethre-Chotzen syndrome?
    Legius E, Fryns JP, Van den Berghe H.
    J Med Genet; 1989 Aug; 26(8):522-4. PubMed ID: 2769726
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  • 7. Clinicogenetic study of Turkish patients with syndromic craniosynostosis and literature review.
    Nur BG, Pehlivanoğlu S, Mıhçı E, Calışkan M, Demir D, Alper OM, Kayserili H, Lüleci G.
    Pediatr Neurol; 2014 May; 50(5):482-90. PubMed ID: 24656465
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  • 8. Roentgencephalometric studies of the premature craniofacial synostoses: report of a family with the Saethre-Chotzen syndrome.
    Pruzansky S, Pashayan H, Kreiborg S, Miller M.
    Birth Defects Orig Artic Ser; 1975 May; 11(2):226-37. PubMed ID: 1227526
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  • 9. Genetic heterogeneity among craniosynostosis syndromes: mapping the Saethre-Chotzen syndrome locus between D7S513 and D7S516 and exclusion of Jackson-Weiss and Crouzon syndrome loci from 7p.
    Lewanda AF, Cohen MM, Jackson CE, Taylor EW, Li X, Beloff M, Day D, Clarren SK, Ortiz R, Garcia C.
    Genomics; 1994 Jan 01; 19(1):115-9. PubMed ID: 8188211
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  • 11. Dermatoglyphics in Saethre-Chotzen syndrome: a family study.
    Borbolla L, Menéndez I.
    Acta Paediatr Hung; 1983 Jan 01; 24(3):269-79. PubMed ID: 6671070
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  • 12. Comparative dermatoglyphic analysis in two types of acrocephalosyndactyly: Saethre-Chotzen syndrome and Pfeiffer syndrome.
    Schaumann B.
    Birth Defects Orig Artic Ser; 1979 Jan 01; 15(6):661-7. PubMed ID: 552891
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  • 13. Are the acrocephalosyndactyly syndromes variable expressions of a single gene defect?
    Escobar V, Bixler D.
    Birth Defects Orig Artic Ser; 1977 Jan 01; 13(3C):139-54. PubMed ID: 890108
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  • 15. Morphology of the foramen magnum in syndromic and non-syndromic brachycephaly.
    Assadsangabi R, Hajmomenian M, Bilaniuk LT, Vossough A.
    Childs Nerv Syst; 2015 May 01; 31(5):735-41. PubMed ID: 25686894
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  • 17. Clinical and genetic analysis of patients with Saethre-Chotzen syndrome.
    de Heer IM, de Klein A, van den Ouweland AM, Vermeij-Keers C, Wouters CH, Vaandrager JM, Hovius SE, Hoogeboom JM.
    Plast Reconstr Surg; 2005 Jun 01; 115(7):1894-902; discussion 1903-5. PubMed ID: 15923834
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  • 18. Crouzon syndrome is not linked to craniosynostosis loci at 7p and 5qter.
    Reardon W, van Herwerden L, Rose C, Jones B, Malcolm S, Winter RM.
    J Med Genet; 1994 Mar 01; 31(3):219-21. PubMed ID: 8014970
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  • 19. Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome.
    Kress W, Schropp C, Lieb G, Petersen B, Büsse-Ratzka M, Kunz J, Reinhart E, Schäfer WD, Sold J, Hoppe F, Pahnke J, Trusen A, Sörensen N, Krauss J, Collmann H.
    Eur J Hum Genet; 2006 Jan 01; 14(1):39-48. PubMed ID: 16251895
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  • 20. Jackson-Weiss syndrome registered in four successive generations. The facies of Crouzon's syndrome with foot abnormalities.
    Stanković B, Krstić V, Stankov B, Jojić L, Nagulić M, Artiko G.
    Doc Ophthalmol; 1994 Jan 01; 85(3):281-6. PubMed ID: 7924855
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