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2003
Mark Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma
Storlazzi, Tiziana ^LU ; Mertens, Fredrik ^LU ; Nascimento, Antonio ; Isaksson, Margareth ^LU ; Wejde, Johan ; Brosjo, Otte ; Mandahl, Nils ^LU and Panagopoulos, Ioannis ^LU (2003) In Human Molecular Genetics 12(18). p.2349-2358
- Contribution to journal › Article
Mark High resolution mapping of an arthritis susceptibility locus on rat chromosome 4, and characterization of regulated phenotypes
Ribbhammar, U ; Flornes, L ; Backdahl, L ; Luthman, Holger ^LU ; Fossum, S and Lorentzen, JC (2003) In Human Molecular Genetics 12(17). p.2087-2096
- Contribution to journal › Article
Mark A genome wide scan for early onset primary hypertension in Scandinavians.
von Wowern, Fredrik ; Bengtsson Boström, Kristina ^LU ; Lindgren, Cecilia ^LU ; Orho-Melander, Marju ^LU ; Fyhrquist, Frej ; Lindblad, Ulf ^LU ; Råstam, Lennart ^LU ; Forsblom, Carol ; Kanninen, Timo and Almgren, Peter ^LU , et al. (2003) In Human Molecular Genetics 12(16). p.2077-2081
- Contribution to journal › Article
2002
Mark Impaired dopamine storage resulting from alpha-synuclein mutations may contribute to the pathogenesis of Parkinson's disease.
Lotharius, Julie ^LU and Brundin, Patrik ^LU (2002) In Human Molecular Genetics 11(20). p.2395-2407
- Contribution to journal › Scientific review
Mark A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.
Buckley, Patrick G. ; Mantripragada, Kiran K. ; Benetkiewicz, Magdalena ; Tapia-Páez, Isabel ; Diaz De Ståhl, Teresita ; Rosenquist, Magnus ; Ali, Haider ; Jarbo, Caroline ; De Bustos, Cecilía and Hirvelä, Carina , et al. (2002) In Human Molecular Genetics 11(25). p.3221-3229
- Contribution to journal › Article
Mark Linkage disequilibrium between polymorphisms in the human TNFRSF1B gene and their association with bone mass in perimenopausal women
Albagha, Omar M E ; Tasker, Paul N ; McGuigan, Fiona E A ^LU ; Reid, David M and Ralston, Stuart H (2002) In Human Molecular Genetics 11(19). p.95-2289
- Contribution to journal › Article
2001
Mark Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13)
Panagopoulos, Ioannis ^LU ; Fioretos, Thoas ^LU ; Isaksson, Margareth ^LU ; Samuelsson, Ulf ; Billström, Rolf ; Strömbeck, Bodil ^LU ; Mitelman, Felix ^LU and Johansson, Bertil ^LU (2001) In Human Molecular Genetics 10(4). p.395-404
- Contribution to journal › Article
Mark X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applications
Sudbrak, Ralf ; Wieczorek, Georg ; Nuber, Ulrike ^LU ; Mann, Wolfgang ; Kirchner, Roland ; Erdogan, Fikret ; Brown, Carolyn J ; Wohrle, Doris ; Sterk, Peter and Kalscheuer, Vera M , et al. (2001) In Human Molecular Genetics 10(1). p.77-83
- Contribution to journal › Article
Mark The mutational spectrum of human malignant autosomal recessive osteopetrosis
Sobacchi, C ; Frattini, A ; Orchard, P ; Porras, O ; Tezcan, I ; Andolina, M ; Babul-Hirji, R ; Baric, I ; Canham, N and Chitayat, D , et al. (2001) In Human Molecular Genetics 10(17). p.1767-1773
- Contribution to journal › Article
Mark DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis
Esteller, Manel ; Fraga, Mario F. ; Guo, Mingzhou ; Garcia-Foncillas, Jesus ; Hedenfalk, Ingrid ^LU ; Godwin, Andrew K. ; Trojan, Joerg ; Vaurs-Barriere, Catherine ; Bignon, Yves-Jean and Ramus, Susan , et al. (2001) In Human Molecular Genetics 10(26). p.3001-3007
- Contribution to journal › Article

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