Associated Papers
A novel mutation in the proteoglycan 4 gene causing CACP syndrome: two sisters report.
Bağrul İ et al.
Pediatric Rheumatology Online Journal, 2023
Pseudo-rheumatic manifestations of limping: Camptodactyly-arthropathy-coxa vara-pericarditis syndrome: Single case report and review of the literature.
Maniscalco V et al.
Frontiers in Pediatrics, 2022
Syndrome of progressive deforming non-inflammatory arthritis of childhood: two patients of camptodactyly-arthropathy-coxa vara-pericarditis syndrome.
Johnson N et al.
Rheumatology International, 2021
What is the right sequencing approach? Solo VS extended family analysis in consanguineous populations.
Alfares A et al.
Bmc Medical Genomics, 2020
32680510 (PubMed )
Supplement: 12920_2020_743_MOESM3_ESM.xlsx › Sheet1
Genotype-phenotype investigation of 35 patients from 11 unrelated families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome.
Yilmaz S et al.
Molecular Genetics & Genomic Medicine, 2018
29397575 (PubMed )
Supplement: MGG3-6-230-s002.xlsx › Appendix2
Camptodactyly-arthropathy-coxavara-pericarditis syndrome in Saudi Arabia: clinical and molecular genetic findings in 22 patients.
Albuhairan I et al.
Seminars in Arthritis and Rheumatism, 2013
Novel PRG4 mutations underlie CACP in Saudi families.
Alazami AM et al.
Human Mutation, 2006
Applying filtration steps to interpret the results of whole-exome sequencing in a consanguineous population to achieve a high detection rate.
Alfares AA
International Journal of Health Sciences, 0
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