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Twelve novel FBN1 mutations in Marfan syndrome and Marfan related phenotypes test the feasibility of FBN1 mutation testing in clinical practice
Halliday, D
,
Hutchinson, S
,
Lonie, L
,
Hurst, J
,
Firth, H
,
Handford, P
,
Wordsworth, P
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http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1735209
Publisher
BMJ Group
Repository
PubMed Central (PMC3 - NLM DTD) (United States)
Keywords
Letter to JMG
Type
Text
Language
English