The locus for combined factor V-factor VIII deficiency (F5F8D) maps to 18q21, between D18S849 and D18S1103

American Journal of Human Genetics

Volumn 61, Issue 1, 1997, Pages 143-150

  Neerman Arbez, M ^a   Antonarakis, S E ^a,b,e   Blouin, J L ^b   Zeinali, S ^c   Akhtari, M ^c   Afshar, Y ^c   Tuddenham, E G D ^d  

^a UNIVERSITY OF GENEVA MEDICAL SCHOOL   (Switzerland)

^b GENEVA UNIVERSITY HOSPITALS   (Switzerland)

^c TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^d MEDICAL RESEARCH COUNCIL   (United Kingdom)

^e Center Médical Universitaire   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BLEEDING DISORDER; BLOOD CLOTTING FACTOR 5 DEFICIENCY; CHROMOSOME 18Q; CLINICAL ARTICLE; DISEASE SEVERITY; DNA POLYMORPHISM; GENETIC VARIABILITY; HEMOPHILIA A; HUMAN; MOLECULAR CLONING; PRIORITY JOURNAL;

IRANIA;

EID: 0030762916     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/513897     Document Type: Article

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