Marfan syndrome with a complex chromosomal rearrangement including deletion of the <it>FBN1 </it>gene
<p>Abstract</p> <p>Background</p> <p>The majority of Marfan syndrome (MFS) cases is caused by mutations in the fibrillin-1 gene (<it>FBN1</it>), mapped to chromosome 15q21.1. Only few reports on deletions including the whole <it>FBN1 </it>gene, d...
Main Authors: | , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2012-01-01
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Series: | Molecular Cytogenetics |
Subjects: | |
Online Access: | http://www.molecularcytogenetics.org/content/5/1/5 |