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

163 related items for PubMed ID: 9182770

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. A variant of Cenani-Lenz syndactyly (CLS): review of the literature and attempt of classification.
    Harpf C, Pavelka M, Hussl H.
    Br J Plast Surg; 2005 Mar; 58(2):251-7. PubMed ID: 15710123
    [Abstract] [Full Text] [Related]

  • 3. Complex toe syndactyly with characteristic facial phenotype: a new syndrome?
    Sobreira NL, Cernach MC, Brunoni D, Perez AB.
    Am J Med Genet A; 2008 Jul 01; 146A(13):1725-8. PubMed ID: 18512233
    [Abstract] [Full Text] [Related]

  • 4. A variant of Cenani-Lenz type syndactyly.
    Seven M, Yüksel A, Ozkiliç A, Elçioğlu N.
    Genet Couns; 2000 Jul 01; 11(1):41-7. PubMed ID: 10756427
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. The duplicated longitudinal epiphysis or "kissing delta phalanx": evolution and variation in three different disorders.
    Elliott AM, Evans JA, Chudley AE, Reed MH.
    Skeletal Radiol; 2004 Jun 01; 33(6):345-51. PubMed ID: 15138725
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Cenani-Lenz syndactyly syndrome - a case report of a family with isolated syndactyly.
    Hettiaracchchi D, Bonnard C, Jayawardana SMA, Ng AYJ, Tohari S, Venkatesh B, Reversade B, Singaraja R, Dissanayake VHW.
    BMC Med Genet; 2018 Jul 24; 19(1):125. PubMed ID: 30041615
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. A case of symbrachydactyly with oligodactyly.
    Seven M, Yuksel A, Ozkilic A.
    Genet Couns; 2001 Jul 24; 12(1):77-83. PubMed ID: 11332981
    [Abstract] [Full Text] [Related]

  • 11. A new form of spondyloperipheral dysplasia with facial dysmorphism, flattened vertebrae, hypoplastic pelvis, brachydactyly and soft tissue syndactyly.
    Kitoh H, Lachman RS.
    Pediatr Radiol; 2001 Jan 24; 31(1):23-6. PubMed ID: 11200993
    [Abstract] [Full Text] [Related]

  • 12. Associated acral and renal malformations: a new syndrome?
    Curran AS, Curran JP.
    Pediatrics; 1972 May 24; 49(5):716-25. PubMed ID: 4402497
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. [Multiple synostosis].
    Czeizel E, Göblyös P.
    Orv Hetil; 1993 Aug 29; 134(35):1917-20. PubMed ID: 8395675
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Autosomal recessive mesoaxial synostotic syndactyly with phalangeal reduction maps to chromosome 17p13.3.
    Malik S, Percin FE, Ahmad W, Percin S, Akarsu NA, Koch MC, Grzeschik KH.
    Am J Med Genet A; 2005 May 01; 134(4):404-8. PubMed ID: 15779011
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.