4 - Bibliothèques de l'Université de Lorraine

103. Lux S.E. ; Tse W.T. ; Menninger J.C. ; John K.M. ; Harri P. ;
Shalev O. ; Chi Icotte R.R. ; Marchesi S.L. ; Watkins P.L. ; Bennet
V. ; Mc Intosch S. ; Collins F.S. ; Franck V. ; Ward D.C. ; Forget
B.G.
Heredytary spherocytosis associated with deletion of human
erythrocyte ankyrin gene on chromosom 8
Nature 1990,345,736-739
104. Pekrun A. ; Eber S.W. ; Kuhlmey A. ; Schrotter W.
Combined ankyrin and spectrin deficiency in hereditary
spherocytosis
Ann Haematol1993, 67, 89-93
105. Savvides P. ; Shalev O. ; John K.M. ; Lux S.E.
Combined spectrin and ankyrin deficiency is common in
autosomal dominant hereditary spherocytosis
Blood 1993,82,2953-2960
106. Miraglia Del Giudice E. ; Francese M. ; Polito R. ; Nobili B. ;
Iolascon A. ; Perotta S.
Apparently normal ankyrin content in unsplenectomized
hereditary spherocytosis patient with the inactivation of one
ankyrin (ANK1) allele
Haematology 1997, 82, 332-333
107. Inoue T. ; Kanzaki A. ; Yawata A. ; Wada H. ; Okamoto N. ;
Takahaschi M. ; Sugihara T. ; Yamada O. ; Yawata Y.
Uniquely higher incidence of isolated or combined deficiency of
band 3 and/or ban 4.2 as pathogenesis of autosomal dominant
inherited hereditary spherocytosis in the japanese population
Int J Hematol1994, 60,227-238