Grønskov, K <br/><br/>
Deletion of all CGG repeats plus flanking sequences in FMR1 does not abolish gene expression.  [electronic resource] 

 -  American journal of human genetics  Oct 1997 
 - 961-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Standard No.: </label>10.1086/514872  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Base Sequence<br/>Female<br/>Fragile X Mental Retardation Protein<br/>Fragile X Syndrome--genetics<br/>Genetic Carrier Screening<br/>Genetic Markers<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Nerve Tissue Proteins--biosynthesis<br/>Pedigree<br/>Polymerase Chain Reaction--methods<br/>Polymorphism, Genetic<br/>RNA-Binding Proteins<br/>Sequence Deletion<br/>Trinucleotide Repeats<br/>X Chromosome