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TitleDateReferenceAuthorsCall #ISSN
Heritability of hemostasis phenotypes and their correlation with type 2 diabetes status in Mexican Americans 2005 Human biology 77 (1): 1-15
  • Anthony Comuzzie
  • Diane M. Warren
  • Jordi Fontcuberta
  • Jose Manuel Soria
  • Juan Carlos Souto
 H6/HB [HUMAN-] 0018-7143
Genetic hematology of French Basques: recent data about this peculiar pyrenean people 2005 International journal of anthropology 20 (3-4): 331-42
  • A. Degioanni
  • F. Bauduer
  • O. Dutour
 H6/HB [INTERNATIONAL-] 0393-9383
Prevalence of eight molecular markers associated with thrombotic diseases in six Amerindian tribes and two African groups of Costa Rica 2004 American journal of human biology 16 (1): 82-6
  • Falko H. Herrmann
  • Gerardo Jiménez-Arce
  • Gudrun Schuster
  • Lizbeth Salazar-Sánchez
  • Rita Grimm
 H6/HB [AMERICAN-] 1042-0533
'The worse hassle is you can't play rugby': haemophilia and masculinity in New Zealand 2000 Current anthropology 41 (3): 443-52
  • Julie Park
 H6 [CURRENT-] 0011-3204
Carrier detection of hemophilia by immunological and coagulation assays in a selected sample of the Mexican population 1997 American journal of human biology 9 (2): 173-8
  • Mercedes Alvarez-Leal
Distribution of F13A phenotypes in Spain: a particularly high frequency of the F13A*2 allele 1992 Human heredity 42 (4): 264-8
  • J L B Caeiro
Haplotype analysis and polymorphic frequency data at two factor IX loci (F9-192 and F9-Hha1) in a Chinese population 1992 Human heredity 42 (3): 204-5
  • S H Chen
Parental origin of factor IX gene mutations, and their distribution in the gene [German sample] 1992 American Journal of human genetics 50 (1): 164-73
  • M Ludwig
Population genetics of coagulation factor XIIIB in three ethnic groups of Singapore 1992 Annals of human biology 19 (3): 277-83
  • N Saha
Factor IX : a deletion-insertion in factor IX gene which abolishes the sequence of the donor junction at the exon IV-intron d splice site 1992 American Journal of human genetics 50 (2): 434-7
  • J Solera
Population genetics of the Malmö polymorphism of coagulation factor IX 1991 Human heredity 41 (6): 391-6
  • A Wallmark
  • 1
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