Chiurazzi, P <br/><br/>
No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome.  [electronic resource] 

 -  American journal of medical genetics  Jul 1994 
 - 309-14 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/ajmg.1320510405  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Fragile X Mental Retardation Protein<br/>Fragile X Syndrome--genetics<br/>Genes--genetics<br/>Genotype<br/>Humans<br/>Intellectual Disability--etiology<br/>Male<br/>Mutation<br/>Nerve Tissue Proteins--biosynthesis<br/>Pedigree<br/>Phenotype<br/>RNA, Messenger--metabolism<br/>RNA-Binding Proteins<br/>X Chromosome