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CODAS syndrome: a new distinct MCA/MR syndrome with radiological changes of spondyloepiphyseal dysplasia. Another case report.
de Almeida, J C; Vargas, F R; Barbosa-Neto, J G; Llerena, J C.
Affiliation
  • de Almeida JC; Unidade de Citogenética Humana, Instituto de Biofísica CCFO, UFRJ, Brazil.
Am J Med Genet ; 55(1): 19-20, 1995 Jan 02.
Article in En | MEDLINE | ID: mdl-7702089
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Collection: 01-internacional Database: MEDLINE Main subject: Osteochondrodysplasias / Abnormalities, Multiple Type of study: Diagnostic_studies Limits: Child, preschool / Female / Humans Language: En Journal: Am J Med Genet Year: 1995 Document type: Article Affiliation country: Brazil Country of publication: United States
Search on Google
Add to My VHL
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Osteochondrodysplasias / Abnormalities, Multiple Type of study: Diagnostic_studies Limits: Child, preschool / Female / Humans Language: En Journal: Am J Med Genet Year: 1995 Document type: Article Affiliation country: Brazil Country of publication: United States