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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

144 related items for PubMed ID: 9072822

  • 21.
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  • 22. Gene symbol: GJA1. Disease: oculodentodigital dysplasia.
    Pontillo A, Flex E, Miertus J.
    Hum Genet; 2005 Feb; 116(3):235. PubMed ID: 15818811
    [No Abstract] [Full Text] [Related]

  • 23. The surgical management of the upper extremity anomalies associated with Du Pan syndrome.
    Lees VC, Hersh JH, Scheker LR.
    J Hand Surg Br; 1998 Feb; 23(1):57-61. PubMed ID: 9571482
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  • 24. Six generations of a family with multiple limb deficiencies.
    Helal A, Perry T, Ogden JA, Greene TL.
    J Pediatr Orthop; 1993 Feb; 13(2):210-3. PubMed ID: 8459013
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  • 25. [The hand-foot-uterus syndrome. A report of a case with recessive autosomal inheritance].
    Stella NC, Triolo O, Corrado F.
    Minerva Ginecol; 1993 Sep; 45(9):429-32. PubMed ID: 8255504
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  • 27. Autosomal dominant tibial hemimelia-polysyndactyly-triphalangeal thumbs syndrome: report of a Brazilian family.
    Richieri-Costa A, de Miranda E, Kamiya TY, Freire-Maia DV.
    Am J Med Genet; 1990 May; 36(1):1-6. PubMed ID: 2333896
    [Abstract] [Full Text] [Related]

  • 28. 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]

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  • 32. The hand-foot-uterus syndrome: a case study.
    Longmuir GA, Conley RN, Nicholson DL, Whitehead M.
    J Manipulative Physiol Ther; 1986 Sep 01; 9(3):213-7. PubMed ID: 3772265
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  • 33.
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  • 34. Mutational analysis of HOXD13 and HOXA13 genes in the triphalangeal thumb-brachyectrodactyly syndrome.
    Pérez-Cabrera A, Kofman-Alfaro S, Zenteno JC.
    J Orthop Res; 2002 Sep 01; 20(5):899-901. PubMed ID: 12382951
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  • 39. Counseling dilemmas in EEC syndrome.
    Tekin M, Ohle C, Johnson DE, Christmas JT, Bodurtha J.
    Genet Couns; 2000 Sep 01; 11(1):19-24. PubMed ID: 10756423
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