Homozygous factor-V mutation as a genetic cause of perinatal thrombosis and cerebral palsy

Developmental Medicine and Child Neurology

Volumn 41, Issue 11, 1999, Pages 777-780

  Harum, Karen H ^a   Hoon Jr , Alexander H ^b   Kato, Gregory J ^b   Casella, James F ^b   Breiter, Steven N ^b   Johnston, Michael V ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 5;

AORTA THROMBOSIS; ARTICLE; BRAIN INFARCTION; CASE REPORT; CEREBRAL PALSY; DOPPLER FLOWMETRY; FEMALE; GENE MUTATION; HOMOZYGOSITY; HUMAN; HUMAN CELL; NUCLEAR MAGNETIC RESONANCE IMAGING; PERINATAL MORBIDITY; PREMATURITY; PRESCHOOL CHILD; PRIORITY JOURNAL; STROKE; THROMBOSIS; VASCULAR LESION;

AORTIC DISEASES; CEREBRAL PALSY; CHILD, PRESCHOOL; CORONARY THROMBOSIS; FACTOR V; FEMALE; HOMOZYGOTE; HUMANS; INFANT, NEWBORN; LEUKOMALACIA, PERIVENTRICULAR; MAGNETIC RESONANCE IMAGING; POINT MUTATION; POLYMERASE CHAIN REACTION;

EID: 0032711382     PISSN: 00121622     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0012162299001541     Document Type: Article

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