Browsing by Author Huisman, Titus Hendrik Jan

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Issue DateTitleAuthor(s)
1972Abnormal hemoglobins in Malta : the significance of two fetal and an adult variantBannister, William H.; Grech, J.L.; Huisman, Titus Hendrik Jan; Schroeder, W.A.
1980Adult and fetal hemoglobin production in erythroid colonies from subjects with β-thalassemia or with hereditary persistence of fetal hemoglobin (HPFH)Huisman, Titus Hendrik Jan; Reese, A. L.; Gravely, Marsha E.; Wilson, Jerry B.; Webber, Brooke B.; Felice, Alex E.
1984Alternate organization of α G-Philadelphia globin genes among US Black and Italian Caucasian heterozygotesSciarratta, Giuseppina V.; Sansone, Gennaro; Ivaldi, Giovanni L.; Felice, Alex E.; Huisman, Titus Hendrik Jan
1977Anomaly in the γ chain heterogeneity of the newbornHuisman, Titus Hendrik Jan; Schroeder, Walter A.; Felice, Alex E.; Powars, Darleen R.; Ringelhann, Bela
1979The association of sickle cell anemia with heterozygous and homozygous α-thalassemia-2 : in vitro HB chain synthesisFelice, Alex E.; Webber, Brooke B.; Miller, Augustus; Mayson, Sylvia M.; Harris, Herman F.; Henson, Jean B.; Gravely, Marsha E.; Huisman, Titus Hendrik Jan
1981Clinical and hematological evaluation of two δ0 δ0 - thalassemia homozygotesDincol, G.; Altay, C.; Aksoy, M.; Gurgey, Aytemiz; Felice, Alex E.; Huisman, Titus Hendrik Jan
1977Detection and quantitation of the fetal hemoglobin variant Hb F-Malta-I in adultsAltay, Gultekin; Garver, Fred A.; Bannister, William H.; Grech, Joseph L.; Huisman, Titus Hendrik Jan; Felice, Alex E.
1986Different ζ globin gene deletions among Black AmericansFelice, Alex E.; Cleek, M. P.; Marino, E. M.; McKie, Kathleen Mood; McKie, Virgil C.; Chang, B. K.; Huisman, Titus Hendrik Jan
1989Hb Evans or α262 (E11) Val→ Metβ2 ; an unstable hemoglobin causing a mild hemolytic anemiaWilson, Jerry B.; Webber, Brooke B.; Kutlar, Abdullah; Reese, A. L.; McKie, Virgil C.; Lutcher, Charles Lawrence; Felice, Alex E.; Huisman, Titus Hendrik Jan
1978Hb Nottingham (α;2β;2 (FG5) 98 VAL→GLY) in a Caucasian male : clinical and biosynthetic studiesOrringer, Eugene P.; Felice, Alex E.; Reese, A. L.; Wilson, Jerry B.; Lam, H. L.; Gravely, Marsha E.; Huisman, Titus Hendrik Jan
1980Hb S, Hb G-Philadelphia and α-thalassemia-2 in a Black familyFelice, Alex E.; Mayson, Sylvia M.; Webber, Brooke B.; Miller, Augustus; Gravely, Marsha E.; Huisman, Titus Hendrik Jan
1982Identification and quantitation of embryonic and three types of fetal hemoglobin produced on induction of the human pluripotent leukemia cell line K‐562 with heminFuhr, Josephy E.; Bamberger, Elena G.; Lozzio, Carmen B.; Lozzio, Bismarck B.; Felice, Alex E.; Altay, Gultekin; Webber, Brooke B.; Reese, A. L.; Mayson, Sylvia M.; Huisman, Titus Hendrik Jan
1980Interaction of the β chain variant hemoglobin Leslie and the α chain variant hemoglobin Montgomery in a Black femaleHuisman, Titus Hendrik Jan; Gravely, Marsha E.; Wilson, Jerry B.; Webber, Brooke B.; Felice, Alex E.; Miller, Augustus
1978Is the trimodality of Hb Leslie (α2β2131Gln→ 0) in heterozygotes the result of a variable number of active α‐chain genes? Evidence for posttranslational control of hemoglobin synthesisFelice, Alex E.; Abraham, Edathara C.; Miller, Augustus; Stallings, M. B.; Huisman, Titus Hendrik Jan
1991The linkage of Hb Valletta [α2β287(F3)Thr→Pro] and Hb F-Malta-I [α2Gγ2117(G19)His→Arg] in the Maltese populationKutlar, Ferdane; Felice, Alex E.; Grech, Joseph L.; Bannister, William H.; Kutlar, Abdullah; Wilson, Jerry B.; Webber, Brooke B.; Hu, Huaiyu; Huisman, Titus Hendrik Jan
1979Observations on the calculated contents of variant and normal α chains in adult and fetal erythrocytesFelice, Alex E.; Huisman, Titus Hendrik Jan
1981The occurrence and identification of α-thalassemia-2 among hemoglobin S heterozygotesFelice, Alex E.; Altay, Cigdem A.; Milner, Paul F.; Huisman, Titus Hendrik Jan
1982Organization of α-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, β-thalassemia, and α-thalassemia-2Felice, Alex E.; Ozdonmez, R.; Headlee, M. E.; Huisman, Titus Hendrik Jan
1984The rare α-Thalassemia-1 of Blacks is a ζα-Thalassemia-1 associated with a deletion of all α- and ζ-Globin genesFelice, Alex E.; Cleek, M. P.; McKie, Kathleen Mood; McKie, Virgil C.; Huisman, Titus Hendrik Jan
1981α-Thalassemia and the production of different α chain variants in heterozygotesFelice, Alex E.; Webber, Brooke B.; Huisman, Titus Hendrik Jan