Hereditary deficiency of vitamin K-dependent coagulation factors with skeletal abnormalities

American Journal of Medical Genetics

Volumn 65, Issue 3, 1996, Pages 241-243

  Boneh, Avihu ^a   Bar Ziv, Jacob ^a  

^a HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

Author keywords

chondrodysplasia punctata; clotting factors; coagulopathy; pseudowarfarin embryopathy; vitamin K

Indexed keywords

BLOOD CLOTTING FACTOR 10; BLOOD CLOTTING FACTOR 7; BLOOD CLOTTING FACTOR 9; PHENOBARBITAL; PHENYTOIN; PROTHROMBIN; VITAMIN K GROUP; WARFARIN;

ARTICLE; BLOOD CLOTTING DISORDER; BONE MALFORMATION; BONE RADIOGRAPHY; BRAIN HEMORRHAGE; CASE REPORT; CHONDRODYSPLASIA; CLINICAL FEATURE; CONVULSION; DISSEMINATED INTRAVASCULAR CLOTTING; FEMALE; HUMAN; INFANT; INTRAMUSCULAR DRUG ADMINISTRATION; ORAL DRUG ADMINISTRATION; PRIORITY JOURNAL; TREATMENT OUTCOME;

BLOOD COAGULATION DISORDERS; BONE AND BONES; FEMALE; HUMANS; INFANT; METABOLISM, INBORN ERRORS; VITAMIN K DEFICIENCY;

EID: 0029902954     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19961028)65:3<241::AID-AJMG13>3.0.CO;2-O     Document Type: Article

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