DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Richards AJ, Yates JR, Williams R. , et al.
A family with Stickler syndrome type 2 has a mutation in the COL11A1 gene resulting in the substitution of glycine 97 by valine in alpha 1 (XI) collagen.
Hum Mol Genet 1996;
5 (09) 1339-1343
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