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

Journal Abstract Search


116 related items for PubMed ID: 19282404

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

  • 2. Congenital duplication of the palm syndrome.
    Al-Qattan MM, Eyaid W, Al-Balwi M.
    Ann Plast Surg; 2007 Sep; 59(3):341-3. PubMed ID: 17721228
    [Abstract] [Full Text] [Related]

  • 3. The WNT7A G204S mutation is associated with both Al-Awadi-Raas Rothschild syndrome and Fuhrmann syndrome phenotypes.
    Al-Qattan MM, Shamseldin HE, Alkuraya FS.
    Gene; 2013 Mar 01; 516(1):168-70. PubMed ID: 23266637
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndrome.
    Franceschini P, Vardeu MP, Dalforno L, Signorile F, Franceschini D, Lala R, Matarazzo P.
    Am J Med Genet; 1992 Dec 01; 44(6):807-12. PubMed ID: 1481852
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 10. [Cryptorchidism with didymo-epididymal dissociation and Robinow's syndrome: 2 case reports].
    Fabbro MA, D'Agostino S, Costa L, Musi L, Cappellari F.
    Pediatr Med Chir; 1997 Dec 01; 19(2):121-4. PubMed ID: 9312747
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. [Statistical analysis of 47 cases with Holt-Qram syndrome].
    Yang JF, Hu DX, Zhou XM.
    Hunan Yi Ke Da Xue Xue Bao; 2001 Jun 28; 26(3):244-6. PubMed ID: 12536695
    [Abstract] [Full Text] [Related]

  • 14. New syndrome: autosomal dominant microcephaly and radio-ulnar synostosis.
    Giuffrè L, Corsello G, Giuffrè M, Piccione M, Albanese A.
    Am J Med Genet; 1994 Jul 01; 51(3):266-9. PubMed ID: 8074157
    [Abstract] [Full Text] [Related]

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

  • 16. No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome.
    Abo-Dalo B, Roes M, Canún S, Delatycki M, Gillessen-Kaesbach G, Hrytsiuk I, Jung C, Kerr B, Mowat D, Seemanova E, Steiner CE, Stewart H, Thierry P, van Buggenhout G, White S, Zenker M, Kutsche K.
    Clin Dysmorphol; 2008 Jul 01; 17(3):181-185. PubMed ID: 18541964
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Developmental biology and classification of congenital anomalies of the hand and upper extremity.
    Oberg KC, Feenstra JM, Manske PR, Tonkin MA.
    J Hand Surg Am; 2010 Dec 01; 35(12):2066-76. PubMed ID: 21134615
    [Abstract] [Full Text] [Related]

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

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 6.