CACP syndrome: identification of five novel mutations and of the first case of UPD in the largest European cohort

Camptodactyly-arthropathy-coxavara-pericarditis syndrome in Saudi Arabia: Clinical and molecular genetic findings in 22 patients

(2013) Intisar Albuhairan et al.   SEMINARS IN ARTHRITIS AND RHEUMATISM

A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract

(2012) Nadia A. Akawi et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

A Novel Deletion Mutation in Proteoglycan-4 Underlies Camptodactyly-Arthropathy-Coxa-Vara-Pericarditis Syndrome in a Consanguineous Pakistani Family

(2011) Sulman Basit et al.   ARCHIVES OF MEDICAL RESEARCH

Rhizomelic chrondrodysplasia punctata type 2 resulting from paternal isodisomy of chromosome 1

(2010) Graeme Nimmo et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Loss of cartilage structure, stiffness, and frictional properties in mice lacking PRG4

(2010) Jeffrey M. Coles et al.   ARTHRITIS AND RHEUMATISM

Achondroplasia: From genotype to phenotype

(2007) Pascal Richette et al.   JOINT BONE SPINE