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. 1994 May;54(5):922–925.

Mutational analysis of the biglycan gene excludes it as a candidate for X-linked dominant chondrodysplasia punctata, dyskeratosis congenita, and incontinentia pigmenti.

S Das, A Metzenberg, G S Pai, J Gitschier
PMCID: PMC1918258  PMID: 8178833

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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