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- 1992
-
Mark
Further characterization of the new marker at DXS115 with regard to carrier detection in hemophilia A
Kling, Stefan LU ; Ljung, Rolf LU
; Sjörin, Elsy
LU
and Nilsson, Inga Marie
(1992)
In Human Genetics
88(4).
p.484-485
- Contribution to journal › Letter
-
Mark
Origin of mutation in sporadic cases of haemophilia-B
Kling, S. LU ; Ljung, R. LU
; Sjörin, Elsy
LU
; Montandon, J.
; Green, P.
; Giannelli, F.
and Nilsson, Inga Marie
(1992)
In European Journal of Haematology
48(3).
p.142-145
- Contribution to journal › Article
-
Mark
Direct estimate of the haemophilia B (factor IX deficiency) mutation rate and of the ratio of the sex-specific mutation rates in Sweden
Montandon, A. J. ; Green, P. M. ; Bentley, D. R. ; Ljung, R. LU
; Kling, S.
LU
; Nilsson, I. M.
and Giannelli, F.
(1992)
In Human Genetics
89(3).
p.319-322
- Contribution to journal › Article
- 1991
-
Mark
Moderate haemophilia B in a female carrier caused by preferential inactivation of the paternal X chromosome
Kling, S. LU ; Coffey, A. J. ; Ljung, R. LU
; Sjörin, Elsy
LU
; Nilsson, Inga Marie
; Holmberg, L.
LU
and Giannelli, F.
(1991)
In European Journal of Haematology
47(4).
p.257-261
- Contribution to journal › Article
-
Mark
More than half the sporadic cases of Hemophilia A in Sweden are due to a recent mutation
Ljung, R. LU
; Kling, S.
LU
; Sjörin, Elsy
LU
and Nilsson, Inga Marie
(1991)
In Acta Paediatrica Scandinavica
80(3).
p.343-348
- Contribution to journal › Article