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35 results
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Prevalence of primary adult lactose malabsorption in three populations of northern China.
Wang YG, Yan YS, Xu JJ, Du RF, Flatz SD, Kühnau W, Flatz G. Wang YG, et al. Among authors: kuhnau w. Hum Genet. 1984;67(1):103-6. doi: 10.1007/BF00270566. Hum Genet. 1984. PMID: 6235167
Distribution of human adult lactose phenotypes in Egypt.
Hussein L, Flatz SD, Kühnau W, Flatz G. Hussein L, et al. Among authors: kuhnau w. Hum Hered. 1982;32(2):94-9. doi: 10.1159/000153266. Hum Hered. 1982. PMID: 6807827
Breath hydrogen test for lactose absorption capacity: importance of timing of hydrogen excretion and of high fasting hydrogen concentration.
Flatz G, Kühnau W, Naftali D. Flatz G, et al. Among authors: kuhnau w. Am J Clin Nutr. 1984 May;39(5):752-5. doi: 10.1093/ajcn/39.5.752. Am J Clin Nutr. 1984. PMID: 6711477
Beja and Nilotes: nomadic pastoralist groups in the Sudan with opposite distributions of the adult lactase phenotypes.
Bayoumi RA, Flatz SD, Kühnau W, Flatz G. Bayoumi RA, et al. Among authors: kuhnau w. Am J Phys Anthropol. 1982 Jun;58(2):173-8. doi: 10.1002/ajpa.1330580208. Am J Phys Anthropol. 1982. PMID: 6810704
Study of alpha-thalassemia in northeastern Thailand at the DNA level.
Hundrieser J, Laig M, Yongvanit P, Sriboonlue P, Sanguansermsri T, Kühnau W, Pape M, Flatz G. Hundrieser J, et al. Among authors: kuhnau w. Hum Hered. 1990;40(2):85-8. doi: 10.1159/000153911. Hum Hered. 1990. PMID: 2335370
Pulmonary hydrogen and methane excretion following ingestion of an unabsorbable carbohydrate: a study of twins.
Flatz G, Czeizel A, Métneki J, Flatz SD, Kühnau W, Jahn D. Flatz G, et al. Among authors: kuhnau w. J Pediatr Gastroenterol Nutr. 1985 Dec;4(6):936-41. doi: 10.1097/00005176-198512000-00014. J Pediatr Gastroenterol Nutr. 1985. PMID: 4067782
Frequency of deletional types of alpha-thalassemia in Kampuchea.
Hundrieser J, Sanguansermsri T, Flatz SD, Kühnau W, Pape M, Papp T, Flatz G. Hundrieser J, et al. Among authors: kuhnau w. Ann Genet. 1988;31(4):205-10. Ann Genet. 1988. PMID: 3265303
Direct demonstration of the HB Suan-Dok mutation in the alpha 2-globin gene by restriction analysis with Sma I.
Hundrieser J, Sanguansermsri T, Laig M, Pape M, Kühnau W, Flatz G. Hundrieser J, et al. Among authors: kuhnau w. Hemoglobin. 1990;14(1):69-77. doi: 10.3109/03630269009002255. Hemoglobin. 1990. PMID: 2384313
A novel missense mutation (Thr176-->Ile) at the putative hinge of the neo N-terminus of activated protein C.
Hallam PJ, Wacey AI, Mannucci PM, Legnani C, Kühnau W, Krawczak M, Kakkar VV, Cooper DN. Hallam PJ, et al. Among authors: kuhnau w. Hum Genet. 1995 Apr;95(4):447-50. doi: 10.1007/BF00208974. Hum Genet. 1995. PMID: 7705844
A paternity case with apparently conflicting multilocus and single-locus DNA typing results.
Kühnau W, Böhm I, Krawczak M, Schmidtke J. Kühnau W, et al. Electrophoresis. 1997 Aug;18(9):1598-601. doi: 10.1002/elps.1150180919. Electrophoresis. 1997. PMID: 9378128
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