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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

191 related items for PubMed ID: 6808331

  • 1. [The Freeman-Sheldon syndrome with mental retardation].
    Cirillo Silengo M, Davi GF, Bianco R, De Marco A, Costa M, Franceschini P, Bonenti G.
    Minerva Pediatr; 1982 Mar 31; 34(6):277-80. PubMed ID: 6808331
    [No Abstract] [Full Text] [Related]

  • 2. Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness.
    Sommer A, Young-Wee T, Frye T.
    Am J Med Genet; 1983 May 31; 15(1):71-7. PubMed ID: 6859126
    [Abstract] [Full Text] [Related]

  • 3. Comments on frontonasal dysplasia, ocular hypertelorism and dystopia canthorum.
    Peterson MQ, Cohen MM, Sedano HO, Frerichs CT.
    Birth Defects Orig Artic Ser; 1971 Jun 31; 7(7):120-4. PubMed ID: 5006144
    [Abstract] [Full Text] [Related]

  • 4. [Hand deformities in Freeman-Sheldon syndrome and their surgical treatment].
    Martini AK, Banniza von Bazan U.
    Z Orthop Ihre Grenzgeb; 1983 Jun 31; 121(5):623-9. PubMed ID: 6649810
    [Abstract] [Full Text] [Related]

  • 5. [49,XXXXX syndrome: apropos of a further case].
    Tumba A, Fryns JP, van OOTEGHEM G, van den Berghe H.
    Union Med Can; 1977 Feb 31; 106(2):226-30. PubMed ID: 847850
    [No Abstract] [Full Text] [Related]

  • 6. 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 31; 28(2):471-5. PubMed ID: 3425620
    [Abstract] [Full Text] [Related]

  • 7. [A rare hand malformation, the Freeman-Sheldon syndrome].
    Freilinger G, Rett A, Killian W.
    Handchirurgie; 1980 Oct 31; 12(3-4):225-7. PubMed ID: 7333533
    [Abstract] [Full Text] [Related]

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  • 10. "C" trigonocephaly syndrome: two additional cases.
    Camera G, Serra G, Selicorni A.
    Am J Med Genet; 1990 Dec 31; 37(4):463-4. PubMed ID: 2260588
    [No Abstract] [Full Text] [Related]

  • 11. Freeman-Sheldon syndrome: a case report.
    Aren G, Yurdabakan Z, Ozcan I.
    Quintessence Int; 2003 Apr 31; 34(4):307-10. PubMed ID: 12731619
    [Abstract] [Full Text] [Related]

  • 12. [On a case of supernumerary metacentric chromosome. Clinical aspects].
    Cagini P, Fallani M, Vasapollo D.
    Minerva Pediatr; 1974 Aug 18; 26(26):1295-301. PubMed ID: 4212722
    [No Abstract] [Full Text] [Related]

  • 13. [The Rubinstein-Taybi syndrome].
    Petrocini S, Cugini A.
    Minerva Pediatr; 1969 Apr 14; 21(15):624-32. PubMed ID: 5402257
    [No Abstract] [Full Text] [Related]

  • 14. A further patient with the Pitt-Rogers-Danks syndrome of mental retardation, unusual face, and intrauterine growth retardation.
    Donnai D.
    Am J Med Genet; 1986 May 14; 24(1):29-32. PubMed ID: 3706410
    [Abstract] [Full Text] [Related]

  • 15. A syndrome of craniofacial, digital, and genital anomalies.
    Harrod MJ, Keele DK, Howard J.
    Birth Defects Orig Artic Ser; 1977 May 14; 13(3B):111-5. PubMed ID: 890088
    [No Abstract] [Full Text] [Related]

  • 16. Intrafamilial variability of Pfeiffer-type cardiocranial syndrome.
    Digilio MC, Marino B, Borzaga U, Giannotti A, Dallapiccola B.
    Am J Med Genet; 1997 Dec 31; 73(4):480-3. PubMed ID: 9415478
    [Abstract] [Full Text] [Related]

  • 17. [Freeman-Sheldon syndrome. Case contribution and review of the literature].
    Parisi G, Molino O, Squadrone NP, Chiarelli A, Jaber H, Galante E.
    Minerva Pediatr; 1991 Oct 31; 43(10):653-9. PubMed ID: 1758388
    [Abstract] [Full Text] [Related]

  • 18. Brachydactyly, mesomelia, mental retardation, aortic dilatation, mitral valve prolapse, and characteristic face.
    Stratton RF, Garcia PR, Young RS, Jorgenson RJ.
    Am J Med Genet; 1993 Apr 15; 46(2):138-41. PubMed ID: 8484398
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