Duplications Involving a Conserved Regulatory Element Downstream of BMP2 Are Associated with Brachydactyly Type A2

Ítems similars

• Identification of Duplication Downstream of BMP2 in a Chinese Family with Brachydactyly Type A2 (BDA2)
  per: Liu, Xudong, et al.
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• Deletion and Point Mutations of PTHLH Cause Brachydactyly Type E
  per: Klopocki, Eva, et al.
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• Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2
  per: Lehmann, Katarina, et al.
  Publicat: (2003)
• A mutation in the receptor binding site of GDF5 causes Mohr‐Wriedt brachydactyly type A2
  per: Kjaer, K W, et al.
  Publicat: (2006)
• Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2
  per: Seemann, Petra, et al.
  Publicat: (2005)