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143 related items for PubMed ID: 6702893

  • 1. The Tel Hashomer camptodactyly syndrome in a consanguineous Brazilian family.
    Gollop TR, Colletto GM.
    Am J Med Genet; 1984 Feb; 17(2):399-406. PubMed ID: 6702893
    [Abstract] [Full Text] [Related]

  • 2. New manifestations observed in the Tel Hashomer camptodactyly syndrome.
    Gollop T, Dal Colletto GM, Ferraretto I, Grimaldi A.
    Prog Clin Biol Res; 1982 Feb; 104():269-77. PubMed ID: 7163271
    [No Abstract] [Full Text] [Related]

  • 3. Camptodactyly, with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases: Tel Hashomer camptodactyly syndrome.
    Goodman RM, Katznelson MB, Hertz M, Katznelson A.
    J Med Genet; 1976 Apr; 13(2):136-41. PubMed ID: 933111
    [Abstract] [Full Text] [Related]

  • 4. The status of dermatoglyphics as a biomarker of Tel Hashomer camptodactyly syndrome: a review of the literature.
    Wijerathne BT, Meier RJ, Agampodi SB.
    J Med Case Rep; 2016 Sep 20; 10(1):258. PubMed ID: 27650795
    [Abstract] [Full Text] [Related]

  • 5. The Tel Hashomer camptodactyly syndrome: report of a new case and review of the literature.
    Pagnan NA, Gollop TR, Lederman H.
    Am J Med Genet; 1988 Feb 20; 29(2):411-7. PubMed ID: 3281460
    [Abstract] [Full Text] [Related]

  • 6. Three new cases of Tel Hashomer camptodactyly syndrome in one Arabic family.
    Tylki-Szymanska A.
    Am J Med Genet; 1986 Mar 20; 23(3):759-63. PubMed ID: 3953674
    [Abstract] [Full Text] [Related]

  • 7. Inguinal hernia and atrial septal defect in Tel Hashomer camptodactyly syndrome: report of a new case expanding the phenotypic spectrum of the disease.
    Franceschini P, Vardeu MP, Signorile F, Testa A, Guala A, Franceschini D, Dalforno L.
    Am J Med Genet; 1993 May 15; 46(3):341-4. PubMed ID: 8488882
    [Abstract] [Full Text] [Related]

  • 8. Autosomal recessive deafness with skeletal dysplasia and facial appearance of Marshall syndrome.
    Miny P, Lenz W.
    Am J Med Genet; 1985 Jun 15; 21(2):317-24. PubMed ID: 4014313
    [Abstract] [Full Text] [Related]

  • 9. Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage (Teebi-Shaltout syndrome): clinical and autopsy findings.
    Froster UG, Rehder H, Höhn W, Oberheuser F.
    Am J Med Genet; 1993 Oct 01; 47(5):717-22. PubMed ID: 8267003
    [Abstract] [Full Text] [Related]

  • 10. Mesomelic limb shortness: a previously unreported autosomal recessive type.
    Reardon W, Hall CM, Slaney S, Huson SM, Connell J, al-Hilaly N, Fixsen J, Baraitser M, Winter RM.
    Am J Med Genet; 1993 Oct 01; 47(5):788-92. PubMed ID: 8267013
    [Abstract] [Full Text] [Related]

  • 11. Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variant.
    Franceschini P, Testa A, Bogetti G, Girardo E, Guala A, Lopez-Bell G, Buzio G, Ferrario E, Piccato E.
    Am J Med Genet; 1992 Jan 01; 42(1):112-6. PubMed ID: 1308349
    [Abstract] [Full Text] [Related]

  • 12. Tibial aplasia-ectrodactyly as variant expression of the Gollop-Wolfgang complex: report of a Brazilian family.
    Richieri-Costa A, Brunoni D, Laredo Filho J, Kasinski S.
    Am J Med Genet; 1987 Dec 01; 28(4):971-80. PubMed ID: 3688036
    [Abstract] [Full Text] [Related]

  • 13. Tel-Hashomer camptodactyly syndrome with hirsuitism in an Indian family.
    Patel ZM, Adhia RA.
    J Assoc Physicians India; 2004 Oct 01; 52():837-8. PubMed ID: 15909866
    [Abstract] [Full Text] [Related]

  • 14. Ectrodactyly and absence (hypoplasia) of the tibia: are there dominant and recessive types?
    Majewski E, Goecke T, Meinecke P.
    Am J Med Genet; 1996 May 03; 63(1):185-9. PubMed ID: 8723107
    [Abstract] [Full Text] [Related]

  • 15. Guadalajara camptodactyly syndrome type I. A corroborative family.
    Figuera LE, Ramírez-Dueñas ML, García-Cruz D, Villar V, Cantú JM.
    Clin Genet; 1993 Jan 03; 43(1):11-5. PubMed ID: 7681735
    [Abstract] [Full Text] [Related]

  • 16. Two siblings with Tel Hashomer camptodactyly and mitral valve prolapse.
    Toriello HV, Higgins JV, Malvitz T, Waterman DF.
    Am J Med Genet; 1990 Aug 03; 36(4):398-403. PubMed ID: 2202212
    [Abstract] [Full Text] [Related]

  • 17. Knobloch syndrome in a large Brazilian consanguineous family: confirmation of autosomal recessive inheritance.
    Passos-Bueno MR, Marie SK, Monteiro M, Neustein I, Whittle MR, Vainzof M, Zatz M.
    Am J Med Genet; 1994 Aug 15; 52(2):170-3. PubMed ID: 7802003
    [Abstract] [Full Text] [Related]

  • 18. Familial transmission of a dysmorphic syndrome: a variant example of Kabuki syndrome?
    Belengeanu V, Rozsnyai K, Farcaş S, Velea I, Fryns JP.
    Genet Couns; 2005 Aug 15; 16(2):167-71. PubMed ID: 16080297
    [Abstract] [Full Text] [Related]

  • 19. Syndactyly type V.
    Robinow M, Johnson GF, Broock GJ.
    Am J Med Genet; 1982 Apr 15; 11(4):475-82. PubMed ID: 6283889
    [Abstract] [Full Text] [Related]

  • 20. Tel Hashomer camptodactyly syndrome: a case report.
    Shah K, Sreekanth R, Thomas B, Danda S.
    West Indian Med J; 2013 Jan 15; 62(1):81-3. PubMed ID: 24171333
    [Abstract] [Full Text] [Related]

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