Literature DB >> 6866038

A familial syndrome of pericarditis, arthritis, and camptodactyly.

M Martínez-Lavín, A Buendía, E Delgado, P Reyes, M C Amigo, J Sabanés, A Zghaib, F Attíe, L Salinas.   

Abstract

Entities:  

Mesh：

Year:  1983        PMID： 6866038     DOI： 10.1056/NEJM198307283090407

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


× No keyword cloud information.
  3 in total

1.  Radiological features in congenital camptodactyly, familial arthropathy and coxa vara syndrome.

Authors:  C Hugosson; S Bahabri; P McDonald; A al-Dalaan; A al-Mazyed
Journal:  Pediatr Radiol       Date:  1994

2.  Camptodactyly, arthropathy, coxa vara, pericarditis (CACP)syndrome: a case report.

Authors:  Byung Ryul Choi; Young Hyo Lim; Kyung Bin Joo; Seung Sam Paik; Nam Su Kim; Je Kyung Lee; Dae Hyun Yoo
Journal:  J Korean Med Sci       Date:  2004-12       Impact factor: 2.153

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

Authors:  Sara Ciullini Mannurita; Marina Vignoli; Lucia Bianchi; Anuela Kondi; Valeria Gerloni; Luciana Breda; Rebecca Ten Cate; Maria Alessio; Angelo Ravelli; Fernanda Falcini; Eleonora Gambineri
Journal:  Eur J Hum Genet       Date:  2013-06-12       Impact factor: 4.246
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.