Takeuchi, H <br/><br/>
Neonatal-onset hereditary coproporphyria with male pseudohermaphrodism.  [electronic resource] 

 -  Blood  Dec 2001 
 - 3871-3 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0006-4971 
<br/><br/><label>Standard No.: </label>10.1182/blood.v98.13.3871  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenal Insufficiency--complications<br/>Adrenocorticotropic Hormone--blood<br/>Base Sequence<br/>Chorionic Gonadotropin<br/>Coproporphyrins--analysis<br/>DNA--chemistry<br/>Deoxyribonuclease HpaII--metabolism<br/>Disorders of Sex Development--complications<br/>Exons<br/>Feces--chemistry<br/>Heterozygote<br/>Humans<br/>Hydrocortisone--blood<br/>Infant, Newborn<br/>Karyotyping<br/>Male<br/>Molecular Sequence Data<br/>Mutation<br/>Pedigree<br/>Polymerase Chain Reaction<br/>Porphyrias, Hepatic--complications<br/>Sequence Analysis, DNA<br/>Testosterone--blood