Colle, M <br/><br/>
[21-Hydroxylase deficiency. Clinical expression of heterozygote carriers in a family].  [electronic resource] 

 -  Archives francaises de pediatrie   
 - 483-5 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0003-9764 
<br/><br/><label>Subjects--Topical Terms: </label><br/>17-alpha-Hydroxyprogesterone<br/>Adolescent<br/>Adrenal Hyperplasia, Congenital--genetics<br/>Androgens--blood<br/>Female<br/>Genetic Carrier Screening--methods<br/>HLA Antigens--analysis<br/>Hirsutism--genetics<br/>Humans<br/>Hydroxyprogesterones--blood<br/>Infant, Newborn<br/>Male<br/>Middle Aged<br/>Pedigree<br/>Steroid 21-Hydroxylase--genetics<br/>Steroid Hydroxylases--deficiency