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Homozygous nonsense mutation in WNT10B and sporadic split-hand/foot malformation (SHFM) with autosomal recessive inheritance
Ariane Blattner, Andreas R. Huber, Benno RöthlisbergerVolume:
152A
Year:
2010
Language:
english
Pages:
4
DOI:
10.1002/ajmg.a.33504
File:
PDF, 138 KB
english, 2010