Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype–phenotype correlations in FBN1 exons 24–40
- 12 January 2001
- journal article
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 9 (1) , 13-21
- https://doi.org/10.1038/sj.ejhg.5200582
Abstract
The European Journal of Human Genetics is the official Journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports, News and Commentary articles and reviews in the rapidly expanding field of human genetics and genomics.Keywords
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