Your browser doesn't support javascript.
loading
Novel B3GALTL mutation in Peters-plus Syndrome.
Dassie-Ajdid, J; Causse, A; Poidvin, A; Granier, M; Kaplan, J; Burglen, L; Doummar, D; Teisseire, P; Vigouroux, A; Malecaze, F; Calvas, P; Chassaing, N.
Clin Genet ; 76(5): 490-2, 2009 Nov.
Article in En | MEDLINE | ID: mdl-19796186
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Galactosyltransferases Limits: Humans / Male Language: En Journal: Clin Genet Year: 2009 Document type: Article Country of publication: Dinamarca
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Galactosyltransferases Limits: Humans / Male Language: En Journal: Clin Genet Year: 2009 Document type: Article Country of publication: Dinamarca