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Clinical and molecular analysis of UAE fibrochondrogenesis patients expands the phenotype and reveals two COL11A1 homozygous null mutations
NA Akawi, L Al-Gazali, BR AliVolume:
82
Year:
2012
Language:
english
Pages:
1
DOI:
10.1111/j.1399-0004.2011.01734.x
File:
PDF, 1.08 MB
english, 2012