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PUBMED FOR HANDHELDS

Journal Abstract Search


128 related items for PubMed ID: 15266625

  • 1. 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]

  • 2. 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]

  • 3. Cooks syndrome: a case report and brief review.
    Brennan CB, Buehler T, Lesher JL.
    Pediatr Dermatol; 2013 Mar 01; 30(4):e52-3. PubMed ID: 22329539
    [Abstract] [Full Text] [Related]

  • 4. Embryology of familial (non-syndromic) brachydactyly of the hand.
    Al-Qattan MM.
    J Hand Surg Eur Vol; 2014 Nov 01; 39(9):926-33. PubMed ID: 24300509
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  • 5. 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 01; 12(4):283-4. PubMed ID: 14564221
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  • 6. Sequence variants in GDF5 and TRPS1 underlie brachydactyly and tricho-rhino-phalangeal syndrome type III.
    Ullah A, Umair M, Hussain S, Jan A, Ahmad W.
    Pediatr Int; 2018 Mar 01; 60(3):304-306. PubMed ID: 29436063
    [No Abstract] [Full Text] [Related]

  • 7. A boy with severe manifestations of type A1 brachydactyly.
    Slavotinek A, Donnai D.
    Clin Dysmorphol; 1998 Jan 01; 7(1):21-7. PubMed ID: 9546826
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  • 10. Concomitance of types D and E brachydactyly: a case report.
    Tülay Koca T, Çiledağ Özdemir F.
    Eur Rev Med Pharmacol Sci; 2015 Dec 01; 19(23):4549-52. PubMed ID: 26698251
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  • 13. 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 01; 164A(9):2398-402. PubMed ID: 24934387
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  • 14. Familial digital arthropathy-brachydactyly.
    Amor DJ, Tudball C, Gardner RJ, Lamandé SR, Bateman JF, Savarirayan R.
    Am J Med Genet; 2002 Mar 15; 108(3):235-40. PubMed ID: 11891693
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  • 15. Hand-foot-genital syndrome - analysis of two cases.
    Piazza MJ, Urbanetz AA.
    JBRA Assist Reprod; 2018 Jun 01; 22(2):157-159. PubMed ID: 29638102
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  • 17. 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 01; 23(4):121-6. PubMed ID: 25144151
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  • 18. Type II familial synpolydactyly: report on two families with an emphasis on variations of expression.
    Al-Qattan MM.
    Eur J Hum Genet; 2011 Jan 01; 19(1):112-4. PubMed ID: 20717165
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  • 20. Brachydactyly type C gene maps to human chromsome 12q24.
    Polymeropoulos MH, Ide SE, Magyari T, Francomano CA.
    Genomics; 1996 Nov 15; 38(1):45-50. PubMed ID: 8954778
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