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Human Genetics|February 1, 1987
X-chromosomally inherited split-hand/split-foot anomaly in a Pakistani kindredM Ahmad, H Abbas, S Haque, et al.
The New England Journal of Medicine|May 6, 1976
Protein patterns of brush-border fragments in congenital lactose malabsorption and in specific hypolactasia of the adultA U Freiburghaus, J Schmitz, M Schindler, et al.
Human Heredity|January 1, 1982
Distribution of human adult lactose phenotypes in EgyptL Hussein, S D Flatz, W Kühnau, et al.
Human Genetics|January 1, 1984
A study of lactose absorption capacity in twinsJ Métneki, A Czeizel, S D Flatz, et al.
Annals of Human Biology|July 1, 1984
Prevalence of primary adult lactose malabsorption in PolandJ Socha, J Ksiazyk, G Flatz, et al.
Hepato-Gastroenterology|June 1, 1980
Intestinal disaccharidase activities and activity ratios in a group of 60 adult German subjectsJ N Howell, J Mellmann, P Ehlers, et al.
Tropical and Geographical Medicine|June 1, 1983
Distribution of adult lactase phenotypes in Bedouins and in urban and agricultural populations of JordanS S Hijazi, A Abulaban, Z Ammarin, et al.
American Journal of Physical Anthropology|June 1, 1982
Beja and Nilotes: nomadic pastoralist groups in the Sudan with opposite distributions of the adult lactase phenotypesR A Bayoumi, S D Flatz, W Kühnau, et al.
Human Genetics|January 1, 1982
Distribution of physiological adult lactase phenotypes, lactose absorber and malabsorber, in GermanyG Flatz, J N Howell, J Doench, et al.
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