4 - Bibliothèques de l'Université de Lorraine

119. Hanspal M. ; Youn J.H. ; Yu H. ; Hanspal J.S. ; Lambert S. ; Palek
J. ; Prchal J.T.
Molecular basis in spectrin and ankyrin deficiencis in severe
hereditary spherocytosis : evidence implïcating a primary
defect of ankyrin
Blood 1991,77,165-173
120. Miraglia Del Giudice E. ; Perotta S. ; Lombardi C. ; Iolascon A.
Decision making at the bedside : diagnosis of hereditary
spherocytosis in a transfused infant
A haematologica 1998, 83, 347-349
121. Eber S.W. ; Gonzales J.M. ; Lux M.L. ; Scarpa A.L. ; Tse W.T. ;
Dornwell M. ; Hebers J. ; Kugler W. ; Forget B.G. ; Lux S.E.
Ankyrin-l mutation is major cause of dominant and recessiv
hereditary spherocytosis
Nat Genet 1996, 13, 214-215
122. Lanciotti M. ; Perutelli P. ; Valetto A. ; Dimartino D. ; Morri P.G.
Ankyrin deficiency in the most common defect in dominant and
non dominant hereditary spherocytosis
Haematologica 1997, 82, 460-462
123. Kanzaki A. ; Takezono M. ; Kaku M. ; Yawata A. ; Ozcan R. ; Kugler
W. ; Eber S.W. ; Yawata Y.
Molecular and genetic characteristics in japanese patients with
hereditary spherocytosis frequent band 3 mutations and rarer
ankyrin mutation
Blood 1997,90 Suppl 1, 66-76