Wang, M <br/><br/>
Double mutant fibrillin-1 (FBN1) allele in a patient with neonatal Marfan syndrome.  [electronic resource] 

 -  Journal of medical genetics  Sep 1996 
 - 760-3 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0022-2593 
<br/><br/><label>Standard No.: </label>10.1136/jmg.33.9.760  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>DNA Mutational Analysis<br/>Exons<br/>Extracellular Matrix Proteins--genetics<br/>Female<br/>Fibrillin-1<br/>Fibrillins<br/>Humans<br/>Infant<br/>Marfan Syndrome--genetics<br/>Microfilament Proteins--genetics<br/>Polymerase Chain Reaction