Wilson, J D <br/><br/>
Familial incomplete male pseudohermaphroditism, type 1. Evidence for androgen resistance and variable clinical manifestations in a family with the Reifenstein syndrome.  [electronic resource] 

 -  The New England journal of medicine  May 1974 
 - 1097-103 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0028-4793 
<br/><br/><label>Standard No.: </label>10.1056/NEJM197405162902001  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Androgen-Insensitivity Syndrome--metabolism<br/>Androgens--metabolism<br/>Androstenedione--metabolism<br/>Child<br/>Child, Preschool<br/>Disorders of Sex Development--blood<br/>Estradiol--metabolism<br/>Estrone--metabolism<br/>Feedback<br/>Follicle Stimulating Hormone--blood<br/>Genes, Recessive<br/>Gynecomastia--genetics<br/>Humans<br/>Hypospadias--genetics<br/>Luteinizing Hormone--blood<br/>Male<br/>Pedigree<br/>Syndrome<br/>Testosterone--biosynthesis