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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

120 related items for PubMed ID: 9212188

  • 1. Brachydactyly in a child with duplication-deficiency subsequent to t(15;20)(q25.2;p12.2)mat. Candidate regions on one or both chromosomes?
    Pfeiffer RA, Kändler C, Sieber E, Rauch A, Trautmann U.
    Clin Genet; 1997 May; 51(5):357-60. PubMed ID: 9212188
    [Abstract] [Full Text] [Related]

  • 2. Liebenberg syndrome: brachydactyly with joint dysplasia (MIM 186550): a second family.
    Tiberio G, Diglio MC, Graziani M, Testa F, Giannotti A.
    J Med Genet; 2000 Jul; 37(7):548-51. PubMed ID: 10970192
    [No Abstract] [Full Text] [Related]

  • 3. Embryology of familial (non-syndromic) brachydactyly of the hand.
    Al-Qattan MM.
    J Hand Surg Eur Vol; 2014 Nov; 39(9):926-33. PubMed ID: 24300509
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  • 4. A 4.6 kb genomic duplication on 20p12.2-12.3 is associated with brachydactyly type A2 in a Chinese family.
    Su P, Ding H, Huang D, Zhou Y, Huang W, Zhong L, Vyse TJ, Wang Y.
    J Med Genet; 2011 May; 48(5):312-6. PubMed ID: 21357617
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  • 5. Holt-Oram syndrome in two generations with translocation t(9;15)(p12;q11.2).
    Caglayan AO, Koklu E, Saatci C, Gunes T, Ozkul Y, Narin N, Baykan A, Dundar M, Buyukkayhan D.
    Ann Saudi Med; 2008 May; 28(3):209-12. PubMed ID: 18500176
    [No Abstract] [Full Text] [Related]

  • 6. De novo apparently balanced reciprocal translocation between 5q11.2 and 17q23 associated with Klippel-Feil anomaly and type A1 brachydactyly.
    Fukushima Y, Ohashi H, Wakui K, Nishimoto H, Sato M, Aihara T.
    Am J Med Genet; 1995 Jul 03; 57(3):447-9. PubMed ID: 7677149
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  • 10. The acrocallosal syndrome and Greig syndrome are not allelic disorders.
    Brueton LA, Chotai KA, van Herwerden L, Schinzel A, Winter RM.
    J Med Genet; 1992 Sep 03; 29(9):635-7. PubMed ID: 1404293
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  • 11. Cerebral defects confirm midline developmental field disturbances in supernumerary der(22), t(11;22) syndrome.
    Pallotta R, Fusilli P, Ehresmann T, Cinti R, Verrotti A, Morgese G.
    Clin Genet; 1996 Nov 03; 50(5):411-6. PubMed ID: 9007334
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  • 12. 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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  • 13. Hand involvement in 13q deletion syndrome.
    Grindel SI, Sandlin C, Wood VE.
    J Pediatr Orthop; 1999 Nov 15; 19(5):620-3. PubMed ID: 10488863
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  • 14. Tibial hemimelia: report on 37 new cases, clinical and genetic considerations.
    Richieri-Costa A, Ferrareto I, Masiero D, da Silva CR.
    Am J Med Genet; 1987 Aug 15; 27(4):867-84. PubMed ID: 3425598
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  • 15. Six generations of a family with multiple limb deficiencies.
    Helal A, Perry T, Ogden JA, Greene TL.
    J Pediatr Orthop; 1993 Aug 15; 13(2):210-3. PubMed ID: 8459013
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  • 19. A chromosomal 5q31.1 gain involving PITX1 causes Liebenberg syndrome.
    Seoighe DM, Gadancheva V, Regan R, McDaid J, Brenner C, Ennis S, Betts DR, Eadie PA, Lynch SA.
    Am J Med Genet A; 2014 Nov 15; 164A(11):2958-60. PubMed ID: 25124102
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  • 20. A novel locus for brachydactyly type A1 on chromosome 5p13.3-p13.2.
    Armour CM, McCready ME, Baig A, Hunter AG, Bulman DE.
    J Med Genet; 2002 Mar 15; 39(3):186-8. PubMed ID: 11897820
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