| 1 | HFG, HOXA13
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| A novel mutation of HOXA13 in a family with hand-foot-genital syndrome and the role of polyalanine expansions in the spectrum of Müllerian fusion anomalies.
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| Jorgensen EM, Ruman JI, Doherty L, Taylor HS.
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| Fertil Steril 94(4):1235-8. doi: 10.1016/j.fertnstert.2009.05.057. Epub 2009 Jul 9.
2010
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| 2 | HFG, HOXA13
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| A novel mutation of HOXA13 in a family with hand-foot-genital syndrome and the role of polyalanine expansions in the spectrum of Müllerian fusion anomalies.
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| Jorgensen EM, Ruman JI, Doherty L, Taylor HS.
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| Fertil Steril 94(4):1235-8. doi: 10.1016/j.fertnstert.2009.05.057. Epub 2009 Jul 9.
2010
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| 3 | HOXA13, HFG
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| Molecular characterization of HOXA13 polyalanine expansion proteins in hand-foot-genital syndrome.
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| Utsch B, McCabe CD, Galbraith K, Gonzalez R, Born M, Dtsch J, Ludwig M, Reutter H, Innis JW.
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| Am J Med Genet A 143(24):3161-8. 2007
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| 4 | HOXA13, HFG
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| Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model.
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| Innis JW, Mortlock D, Chen Z, Ludwig M, Williams ME, Williams TM, Doyle CD, Shao Z, Glynn M, Mikulic D, Lehmann K, Mundlos S, Utsch B.
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| Hum Mol Genet 13(22):2841-51. Epub 2004 Sep 22. 2004
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| 5 | HFG, HOXA13
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| A novel stable polyalanine [poly(A)] expansion in the HOXA13 gene associated with hand-foot-genital syndrome: proper function of poly(A)-harbouring transcription factors depends on a critical repeat length?
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| Utsch B, Becker K, Brock D, Lentze MJ, Bidlingmaier F, Ludwig M.
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| Hum Genet 110(5):488-94. Review. 2002
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| 6 | DEL2Q31,HFG,HOXA@,HOXB@,HOXC@,HOXD@,PSDY2,SDTY5
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| Limb malformations and the human HOX genes.
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| Goodman FR.
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| Am J Med Genet 112(3):256-65. Review. 2002
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| 7 | HFG, HOXA13
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| Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome.
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| Goodman FR, Bacchelli C, Brady AF, Brueton LA, Fryns JP, Mortlock DP, Innis JW, Holmes LB, Donnenfeld AE, Feingold M, Beemer FA, Hennekam RC, Scambler PJ.
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| Am J Hum Genet 67(1):197-202. 2000
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| 8 | HFG, HOXA@
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| Haploinsufficiency of the HOXA Gene Cluster, in a Patient with Hand-Foot-Genital Syndrome, Velopharyngeal Insufficiency, and Persistent Patent Ductus Botalli.
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| Devriendt K, et al.
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| Am J Hum Genet 65(1):249-251. No abstract available 1999
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| 9 | HFG, HOXA13
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| Mutation of HOXA13 in hand-foot-genital syndrome.
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| Mortlock DP, et al.
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| Nat Genet 15 : 179-180. 1997
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