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Updated: Jun 6, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

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Symmetrical enchondromatosis is associated with duplication of 12p11.23 to 12p11.22 including PTHLH

Morag Collinson1, Samantha J Leonard, Jocelyn Charlton

  • 1Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, Wiltshire, UK.

American Journal of Medical Genetics. Part A
|November 18, 2010
PubMed

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