71 – 78 of 78
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=""
width=""
height=""
allowtransparency="true"
frameborder="0">
</iframe>
- 1998
-
Mark
NAGLU mutations underlying Sanfilippo syndrome type B
- Contribution to journal › Article
- 1997
-
Mark
Molecular/structural characterization of novel mutations and identification of novel polymorphisms in the Bruton's tyrosine kinase (Btk) gene from patients with X-linked agammaglobulinemia (XLA).
Saha, BK ; Curtis, SK ; Vogler, LB and Vihinen, Mauno LU
(1997)
In American Journal of Human Genetics
61(4).
p.345-345
- Contribution to journal › Published meeting abstract
-
Mark
Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: Paucity of mutations in the coding region, but splice defects in two families
Fujita, Ricardo ; Buraczynska, Monika ; Gieser, Linn ; Wu, Weiping ; Forsythe, Patricia ; Abrahamson, Magnus LU
; Jacobsson, Samuel G
; Sieving, Paul A
; Andréasson, Sten
LU
and Swaroop, Anand
(1997)
In American Journal of Human Genetics
61(3).
p.571-580
- Contribution to journal › Article
-
Mark
Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer
Hakansson, Sara ; Johannsson, O LU ; Johansson, Ulla LU ; Sellberg, G LU ; Loman, N LU ; Gerdes, A M ; Holmberg, E ; Dahl, N ; Pandis, N and Kristoffersson, U LU
, et al.
(1997)
In American Journal of Human Genetics
60(5).
p.1068-1078
- Contribution to journal › Article
-
Mark
Family cell lines available for research - An endangered resource? [7]
Lernmark, A. LU
; Eisenbarth, George
; Ducat, lee
; Erlich, Henry
; Faustman, Denise
; Maclaren, Noel
; Ott, Jurg
; Permutt, M. Alan
; She, Jin-Xiong
and Todd, John
(1997)
In American Journal of Human Genetics
61(3).
p.778-779
- Contribution to journal › Letter
- 1996
-
Mark
Founding BRCA1 Mutations in Hereditary Breast and Ovarian Cancer in Southern Sweden
Johannsson, Oscar Thor ; Ostermeyer, E.A. ; Hakansson, S. ; Friedman, L.S. ; Johansson, U. ; Sellberg, Gunilla LU ; Brondum Nielsen, K. ; Sele, V. ; Olsson, Håkan LU
and King, M-C.
, et al.
(1996)
In American Journal of Human Genetics
58(3).
p.441-450
- Contribution to journal › Article
- 1993
-
Mark
HLA-DQ primarily confers protection and HLA-DR susceptibility in type I (insulin-dependent) diabetes studied in population-based affected families and controls
Kockum, I. ; Wassmuth, R. ; Holmberg, E. ; Michelsen, B. and Lernmark, A. LU
(1993)
In American Journal of Human Genetics
53(1).
p.150-167
- Contribution to journal › Article
- 1988
-
Mark
The Malmo polymorphism of coagulation factor IX, an immunologic polymorphism due to dimorphism of residue 148 that is in linkage disequilibrium with two other F.IX polymorphisms
Graham, J. B. ; Lubahn, D. B. ; Lord, S. T. ; Kirshtein, J. ; Nilsson, Inga Marie ; Wallmark, A. LU ; Ljung, R. LU
; Frazier, L. D.
; Ware, J. L.
and Wah Lin, S.
, et al.
(1988)
In American Journal of Human Genetics
42(4).
p.573-580
- Contribution to journal › Article