Mutation of HOXA13 in hand-foot-genital syndrome. Mortlock DP, Innis JW (1997) Nat Genet 15: 179-80 Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome. 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 (2000) Am J Hum Genet 67: 197-202 Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model. 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 (2004) Hum Mol Genet 13: 2841-51 A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome. Innis JW, Goodman FR, Bacchelli C, Williams TM, Mortlock DP, Sateesh P, Scambler PJ, McKinnon W, Guttmacher AE (2002) Hum Mutat 19: 573-4 Limb development: molecular dysmorphology is at hand! Innis JW, Mortlock DP (1998) Clin Genet 53: 337-48
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