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Yang Ao Selected Research

type 2 Syndactyly

2/2007Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome.
2/2005[HOXD13 polyalanine tract expansion in synpolydactyly: mutation detection and prenatal diagnosis in a large Chinese family].

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Yang Ao Research Topics

Disease

2type 2 Syndactyly
02/2007 - 02/2005
1Syndactyly (Polysyndactyly)
02/2007
1Brachydactyly
02/2007
1type v Syndactyly
02/2007
1Dyschromatosis symmetrica hereditaria 1
04/2004
1Neoplasms (Cancer)
12/2003
1Carcinoma (Carcinomatosis)
12/2003

Drug/Important Bio-Agent (IBA)

2polyalanineIBA
02/2007 - 02/2005
2DNA (Deoxyribonucleic Acid)IBA
02/2007 - 12/2003
1Glutamine (L-Glutamine)FDA Link
02/2007
1Adenosine DeaminaseIBA
04/2004
1RNA (Ribonucleic Acid)IBA
04/2004