Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Hazel Camoens"'
Publikováno v:
Transfusion. 33:963-963
Autor:
Hazel Camoens, A.J. Baxi
Publikováno v:
Human Heredity. 19:65-70
Autor:
K. Berg, Hazel Camoens
Publikováno v:
Vox Sanguinis. 24:283-286
A normal serum with haemolytic and agglutinating activity against trypsintreated red blood cells at 37°C has been studied. The properties of this serum appear to be very similar, if not identical, to those of the warm haemolysin described by Heisto
Autor:
Hazel Camoens
Publikováno v:
Human Heredity. 21:297-301
199 blood samples from India were screened for their AK types. 160 persons were found to be AK 1–1, and 39 2–1. No sample of the type 2–2 was observed. Differences with study respect to AK gene distribution in an Indian, Norwegian, Chinese and
Autor:
A. Warlow, M. Lahav, H. Sørensen, N.D. Carter, G. Tusnady, J. Dissing, C. Ropartz, L.C. Legueult, I. Persson, K. Ohkura, L. Rivat, G. Beckman, K. Berg, H. Gershowitz, M.S. Adams, T.M. Allan, N. Myrberg, A. Pellicer, D.P. Agarwal, V. Bhalla, James J. Nora, S. Singh, J. Lund, G. Berlin, H.R. Maricq, K. Kølendorf, Anil K. Sinha, L. Beckman, Luan Eng Lie-Injo, Liliane Rivat, S.S. Magnússon, S. Ashbel, L. Kølendorf, L.R. Weitkamp, P.H. Alsbirk, A.W. Eriksson, P.T. Rowley, E. Monn, M.S. Schanfield, B. Sela, B. Bonné, Benkmann Hg, H. Walter, A. Szeinberg, H.-G. Benkmann, K.E. Alsbirk, Q.B. Welch, A. Czeizel, A.R. Coward, L. Hirth, Sen Pathak, Hazel Camoens, A.E. Mourant, C.J. Brackenridge, T. Pellicer, T.E.B. Leakey, P.Y. Rousseau, H. Arvilommi, R. Ananthakrishnan, M. Stahn, H.W. Goedde, L. Tsacheva
Publikováno v:
Human Heredity. 22:I-VIII
Autor:
K. Berg, A. Pellicer, H. Gershowitz, M. Stahn, T.M. Allan, Anil K. Sinha, James J. Nora, Sen Pathak, S. Singh, G. Berlin, Liliane Rivat, G. Tusnady, H. Arvilommi, B. Sela, A. Czeizel, E. Monn, L.R. Weitkamp, H. Sørensen, M.S. Schanfield, S.S. Magnússon, N. Myrberg, L. Rivat, K.E. Alsbirk, J. Dissing, T.E.B. Leakey, B. Bonné, Luan Eng Lie-Injo, T. Pellicer, M.S. Adams, P.Y. Rousseau, H.-G. Benkmann, R. Ananthakrishnan, L. Beckman, Q.B. Welch, V. Bhalla, N.D. Carter, C.J. Brackenridge, A.R. Coward, C. Ropartz, L. Hirth, L. Kølendorf, Hazel Camoens, A. Warlow, Benkmann Hg, M. Lahav, J. Lund, P.H. Alsbirk, L. Tsacheva, P.T. Rowley, A.E. Mourant, H.R. Maricq, K. Kølendorf, I. Persson, H.W. Goedde, G. Beckman, S. Ashbel, A.W. Eriksson, H. Walter, A. Szeinberg, D.P. Agarwal, L.C. Legueult, K. Ohkura
Publikováno v:
Human Heredity. 22:601-603