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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

286 related items for PubMed ID: 22329539

  • 1. Cooks syndrome: a case report and brief review.
    Brennan CB, Buehler T, Lesher JL.
    Pediatr Dermatol; 2013; 30(4):e52-3. PubMed ID: 22329539
    [Abstract] [Full Text] [Related]

  • 2. Brachydactyly type B with its distinct facies and 'Cooks syndrome' are the same entity.
    de Ravel TJ, Berkowitz DE, Wagner JM, Jenkins T.
    Clin Dysmorphol; 1999 Jan; 8(1):41-5. PubMed ID: 10327250
    [Abstract] [Full Text] [Related]

  • 3. Anonychia and absence/hypoplasia of distal phalanges (Cooks syndrome): report of a second family.
    Nevin NC, Thomas PS, Eedy DJ, Shepherd C.
    J Med Genet; 1995 Aug; 32(8):638-41. PubMed ID: 7473658
    [Abstract] [Full Text] [Related]

  • 4. A novel patient with Cooks syndrome supports splitting from "classic" brachydactyly type B.
    Castori M, Brancati F, Mingarelli R, Mundlos S, Dallapiccola B.
    Am J Med Genet A; 2007 Jan 15; 143A(2):195-9. PubMed ID: 17163524
    [Abstract] [Full Text] [Related]

  • 5. Catel-Manzke syndrome without cleft palate: a case report.
    Puri RD, Phadke SR.
    Clin Dysmorphol; 2003 Oct 15; 12(4):279-81. PubMed ID: 14564220
    [Abstract] [Full Text] [Related]

  • 6. Fibular aplasia, tibial campomelia, and oligosyndactyly: a further patient with a 2-year follow-up.
    Sezer O, Gebesoglu I, Yuan B, Karaca E, Gokce E, Gunes S.
    Clin Dysmorphol; 2014 Oct 15; 23(4):121-6. PubMed ID: 25144151
    [No Abstract] [Full Text] [Related]

  • 7. Unusual combination of limb malformations in the same patient: brachydactyly with syndactyly and postaxial polydactyly of the hands and postaxial oligodactyly of the feet.
    Ferda Percin E, Yilmaz S.
    Clin Dysmorphol; 2003 Oct 15; 12(4):283-4. PubMed ID: 14564221
    [Abstract] [Full Text] [Related]

  • 8. Severe manifestations of hand-foot-genital syndrome associated with a novel HOXA13 mutation.
    Imagawa E, Kayserili H, Nishimura G, Nakashima M, Tsurusaki Y, Saitsu H, Ikegawa S, Matsumoto N, Miyake N.
    Am J Med Genet A; 2014 Sep 15; 164A(9):2398-402. PubMed ID: 24934387
    [Abstract] [Full Text] [Related]

  • 9. A boy with severe manifestations of type A1 brachydactyly.
    Slavotinek A, Donnai D.
    Clin Dysmorphol; 1998 Jan 15; 7(1):21-7. PubMed ID: 9546826
    [Abstract] [Full Text] [Related]

  • 10. An unusual family with brachydactyly.
    Silva EO.
    Am J Med Genet A; 2003 Mar 01; 117A(2):191-3. PubMed ID: 12567422
    [No Abstract] [Full Text] [Related]

  • 11. Is brachydactyly type Ballard a variant of brachydactyly type E?
    Jensen K, Hoo JJ.
    Am J Med Genet A; 2004 Aug 15; 129A(1):95-7. PubMed ID: 15266625
    [No Abstract] [Full Text] [Related]

  • 12. An autopsy case of Adams-Oliver syndrome.
    Jun SY, Khang SK, Park SH.
    J Korean Med Sci; 2000 Aug 15; 15(4):482-4. PubMed ID: 10983704
    [Abstract] [Full Text] [Related]

  • 13. Symbrachydactyly involving both the hand and foot. A report of two cases.
    Uchida T, Kojima T, Hirakawa M, Uchida M.
    Handchir Mikrochir Plast Chir; 1995 Jan 15; 27(1):51-4. PubMed ID: 7705729
    [Abstract] [Full Text] [Related]

  • 14. [A case of congenital hypodactyly of the hand and foot].
    Mamedov AG, Seidov MM.
    Ortop Travmatol Protez; 1991 Apr 15; (4):51-2. PubMed ID: 1754179
    [No Abstract] [Full Text] [Related]

  • 15. Hands and feet in the Apert syndrome.
    Cohen MM, Kreiborg S.
    Am J Med Genet; 1995 May 22; 57(1):82-96. PubMed ID: 7645606
    [Abstract] [Full Text] [Related]

  • 16. Two isolated cases with symmetrically absent hands and feet.
    Horn D, Kolb GP.
    Clin Dysmorphol; 1994 Jul 22; 3(3):228-33. PubMed ID: 7981858
    [Abstract] [Full Text] [Related]

  • 17. Clinical and molecular studies of brachydactyly type D.
    Robin NH, Hurvitz J, Warman ML, Morrison S.
    Am J Med Genet; 1999 Aug 06; 85(4):413-8. PubMed ID: 10398270
    [Abstract] [Full Text] [Related]

  • 18. Mesoaxial complete syndactyly and synostosis with hypoplastic thumbs: an unusual combination or homozygous expression of syndactyly type I?
    Percin EF, Percin S, Egilmez H, Sezgin I, Ozbas F, Akarsu AN.
    J Med Genet; 1998 Oct 06; 35(10):868-74. PubMed ID: 9783716
    [Abstract] [Full Text] [Related]

  • 19. Choledochal cyst associated with rare hand malformation.
    Dudin A, Abdelshafi M, Rambaud-Cousson A.
    Am J Med Genet; 1995 Mar 27; 56(2):161-3. PubMed ID: 7625438
    [Abstract] [Full Text] [Related]

  • 20. Cenani-Lenz syndrome: report of a new case and review of the literature.
    Nezarati MM, McLeod DR.
    Clin Dysmorphol; 2002 Jul 27; 11(3):215-8. PubMed ID: 12072805
    [Abstract] [Full Text] [Related]

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