Genetic Disorders of Bilirubin Metabolism

reportActive / Technical Report | Accession Number: AD0753375 | Open PDF

Abstract:

Chronic idiopathic jaundice and three other entities that share the features of familial disorders of bilirubin metabolism in the absence of hemolytic disease or obstruction of bile passages are discussed.

Author(s):
Johnson, Frank B.
Author Organization(s):
ARMED FORCES INST OF PATHOLOGY WASHINGTON DC
Supplementary Note:
Availability: Pub. in The Liver: International Academy of Pathology Monograph, n13 ch2 p12-20 1972.
Pagination:
0010

Security Markings

DOCUMENT & CONTEXTUAL SUMMARY

Distribution:
Approved For Public Release, Document Partially Illegible
Distribution Statement:
Approved For Public Release; Distribution Is Unlimited. Document Partially Illegible.

RECORD

Collection: TR
Identifying Numbers
Monitor Series:
AFIP
 Subject Terms
Joint Capability Areas:
JCA_1.4.1_Force Health Protection; JCA_1.4_Force Support; JCA_6_Net Centric; JCA_1.2.5_Lessons Learned; JCA_6.3.3_Spectrum Management; JCA_6.4.1_Secure Information Exchange; JCA_1.3_Human Capital Management; JCA_1_Force Support
Communities of Interest:
Materials and Manufacturing Processes
Descriptor(s):
*GENETICS, *METABOLIC DISEASES, *BILE PIGMENTS, REPRINTS, DISEASES, BILIARY SYSTEM, HISTOLOGY, PATHOLOGY, LIVER
Field(s)/Group(s):
Medicine and Medical Research
Keyword(s):
JAUNDICE
Report Date:
1971 Jan 01