Stewart, C J R <br/><br/>
Detection of Y-chromosome in gonadal tumours using fluorescence in situ hybridization: diagnostic value in intersex conditions including older patients with clinically unsuspected androgen insensitivity syndrome.  [electronic resource] 

 -  Histopathology  Jan 2008 
 - 175-82 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1365-2559 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2559.2007.02927.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenoma--diagnosis<br/>Adolescent<br/>Adult<br/>Aged<br/>Androgen-Insensitivity Syndrome--diagnosis<br/>Biopsy<br/>Chromosomes, Human, Y--genetics<br/>Disorders of Sex Development--diagnosis<br/>Dysgerminoma--diagnosis<br/>Female<br/>Genes, sry--genetics<br/>Gonadoblastoma--diagnosis<br/>Humans<br/>In Situ Hybridization, Fluorescence--methods<br/>Male<br/>Middle Aged<br/>Ovarian Neoplasms--diagnosis<br/>Phenotype<br/>Sensitivity and Specificity<br/>Sertoli Cell Tumor--diagnosis