These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

215 related items for PubMed ID: 3425620

  • 1. Further evidence for genetic heterogeneity of whistling face or Freeman-Sheldon syndrome in a Chinese family.
    Wang TR, Lin SJ.
    Am J Med Genet; 1987 Oct; 28(2):471-5. PubMed ID: 3425620
    [Abstract] [Full Text] [Related]

  • 2. [The Freeman-Sheldon Syndrome].
    Aldinger G, Eulert J.
    Z Orthop Ihre Grenzgeb; 1983 Oct; 121(5):630-3. PubMed ID: 6649811
    [Abstract] [Full Text] [Related]

  • 3. Autosomal recessive form of whistling face syndrome in sibs.
    Dallapiccola B, Giannotti A, Lembo A, Saguì L.
    Am J Med Genet; 1989 Aug; 33(4):542-4. PubMed ID: 2596515
    [Abstract] [Full Text] [Related]

  • 4. New evidence for genetic heterogeneity of the Freeman-Sheldon syndrome.
    Sánchez JM, Kaminker CP.
    Am J Med Genet; 1986 Nov; 25(3):507-11. PubMed ID: 3789012
    [Abstract] [Full Text] [Related]

  • 5. Freeman-Sheldon syndrome: a case report.
    Aren G, Yurdabakan Z, Ozcan I.
    Quintessence Int; 2003 Apr; 34(4):307-10. PubMed ID: 12731619
    [Abstract] [Full Text] [Related]

  • 6. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: a new autosomal recessive syndrome.
    Richieri-Costa A, Pereira SC.
    Am J Med Genet; 1992 Mar 01; 42(5):681-7. PubMed ID: 1632438
    [Abstract] [Full Text] [Related]

  • 7. Whistling face (Freeman-Sheldon) syndrome in two siblings.
    Bekir N, Bayraktaroğlu Z, Coşkun Y, Karaaslan C.
    Turk J Pediatr; 1994 Mar 01; 36(4):329-32. PubMed ID: 7825240
    [Abstract] [Full Text] [Related]

  • 8. [A rare hand malformation, the Freeman-Sheldon syndrome].
    Freilinger G, Rett A, Killian W.
    Handchirurgie; 1980 Mar 01; 12(3-4):225-7. PubMed ID: 7333533
    [Abstract] [Full Text] [Related]

  • 9. Autosomal recessive type of whistling face syndrome in twins.
    Kousseff BG, McConnachie P, Hadro TA.
    Pediatrics; 1982 Mar 01; 69(3):328-31. PubMed ID: 7199706
    [Abstract] [Full Text] [Related]

  • 10. Freeman-Sheldon syndrome. A case report and review of the literature.
    Ferrari D, Bettuzzi C, Donzelli O.
    Chir Organi Mov; 2008 Sep 01; 92(2):127-31. PubMed ID: 18677448
    [Abstract] [Full Text] [Related]

  • 11. Craniocarpotarsal dysplasia: the whistling face syndrome.
    Guyuron B, Winkler PA.
    Ann Plast Surg; 1988 Jan 01; 20(1):86-8. PubMed ID: 3341720
    [Abstract] [Full Text] [Related]

  • 12. [Freeman-Sheldon syndrome: clinical manifestations and anesthetic and surgical management].
    Alonso Calderón JL, Ali Taoube K.
    An Esp Pediatr; 2002 Feb 01; 56(2):175-9. PubMed ID: 11827658
    [Abstract] [Full Text] [Related]

  • 13. Report on two cases of Freeman-Sheldon syndrome ("whistling face).
    Savini R, Gualdrini G.
    Ital J Orthop Traumatol; 1980 Apr 01; 6(1):105-15. PubMed ID: 7203992
    [Abstract] [Full Text] [Related]

  • 14. Whistling face syndrome. A case report and literature review.
    Millner MM, Mutz ID, Rosenkranz W.
    Acta Paediatr Hung; 1991 Apr 01; 31(3):279-89. PubMed ID: 1742043
    [Abstract] [Full Text] [Related]

  • 15. [Hand deformities in Freeman-Sheldon syndrome and their surgical treatment].
    Martini AK, Banniza von Bazan U.
    Z Orthop Ihre Grenzgeb; 1983 Apr 01; 121(5):623-9. PubMed ID: 6649810
    [Abstract] [Full Text] [Related]

  • 16. The Bartsocas-Papas syndrome: autosomal recessive form of popliteal pterygium syndrome in a male infant.
    Papadia F, Zimbalatti F, La Rosa CG.
    Am J Med Genet; 1984 Apr 01; 17(4):841-7. PubMed ID: 6720749
    [Abstract] [Full Text] [Related]

  • 17. [Cranio-carpo-tarsal dysplasia syndrome (Freeman-Sheldon syndrome, whistling face syndrome)].
    Träger D.
    Z Orthop Ihre Grenzgeb; 1987 Apr 01; 125(1):106-7. PubMed ID: 3577337
    [Abstract] [Full Text] [Related]

  • 18. [Anesthetic management of a patient with Freeman-Sheldon syndrome].
    Yamamoto S, Osuga T, Okada M, Hashimoto T, Shigematsu H, Suzuki S, Fujita K, Matsumoto N, Hori T.
    Masui; 1994 Nov 01; 43(11):1748-53. PubMed ID: 7861610
    [Abstract] [Full Text] [Related]

  • 19. Autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfeet in male patients.
    Richieri-Costa A, Pereira SC.
    Am J Med Genet; 1993 Oct 01; 47(5):707-9. PubMed ID: 8267000
    [Abstract] [Full Text] [Related]

  • 20. Newly recognized autosomal recessive faciothoracoskeletal syndrome.
    Richieri-Costa A, Guion-Almeida ML, Lauris JR, Ferreira DM.
    Am J Med Genet; 1994 Jan 15; 49(2):224-8. PubMed ID: 8116673
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.