Germain, D <br/><br/>
Fluorescence-assisted mismatch analysis (FAMA) for exhaustive screening of the alpha-galactosidase A gene and detection of carriers in Fabry disease.  [electronic resource] 

 -  Human genetics  Dec 1996 
 - 719-26 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/s004390050292  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Child, Preschool<br/>Exons<br/>Fabry Disease--genetics<br/>Female<br/>Genetic Carrier Screening--methods<br/>Genetic Techniques<br/>Humans<br/>Male<br/>Middle Aged<br/>Point Mutation<br/>Promoter Regions, Genetic<br/>Sequence Deletion<br/>alpha-Galactosidase--genetics