Layman, L C <br/><br/>
The Finnish follicle-stimulating hormone receptor gene mutation is rare in North American women with 46,XX ovarian failure.  [electronic resource] 

 -  Fertility and sterility  Feb 1998 
 - 300-2 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article 
<br/><br/><label>ISSN: </label>0015-0282 
<br/><br/><label>Standard No.: </label>10.1016/s0015-0282(97)00480-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Alleles<br/>DNA--analysis<br/>Diploidy<br/>Electrophoresis, Polyacrylamide Gel<br/>Ethnicity<br/>Female<br/>Finland<br/>Humans<br/>North America<br/>Point Mutation--genetics<br/>Polymerase Chain Reaction<br/>Primary Ovarian Insufficiency--ethnology<br/>Receptors, FSH--genetics