Grasso, M <br/><br/>
Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients.  [electronic resource] 

 -  American journal of medical genetics  Jul 1999 
 - 311-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Standard No.: </label>10.1002/(sici)1096-8628(19990730)85:3<311::aid-ajmg24>3.0.co;2-a  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Blotting, Southern<br/>Blotting, Western<br/>DNA--chemistry<br/>DNA Mutational Analysis<br/>Female<br/>Fragile X Mental Retardation Protein<br/>Fragile X Syndrome--genetics<br/>Humans<br/>Male<br/>Mosaicism<br/>Mutation<br/>Nerve Tissue Proteins--genetics<br/>RNA-Binding Proteins<br/>Sequence Deletion<br/>Trinucleotide Repeats--genetics