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2010
Mark A Missense Mutation in the Aggrecan C-type Lectin Domain Disrupts Extracellular Matrix Interactions and Causes Dominant Familial Osteochondritis Dissecans
Stattin, Eva-Lena ; Wiklund, Fredrik ; Lindblom, Karin ^LU ; Önnerfjord, Patrik ^LU ; Jonsson, Bjorn-Anders ; Tegner, Yelverton ; Sasaki, Takako ; Struglics, André ^LU ; Lohmander, Stefan ^LU and Dahl, Niklas , et al. (2010) In American Journal of Human Genetics 86(2). p.126-137
- Contribution to journal › Article
2009
Mark Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa
Friedman, James S. ; Ray, Joseph W. ; Waseem, Naushin ; Johnson, Kory ; Brooks, Matthew J. ; Hugosson, Therése ^LU ; Breuer, Debra ; Branham, Kari E. ; Krauth, Daniel S. and Bowne, Sara J. , et al. (2009) In American Journal of Human Genetics 84(6). p.792-800
- Contribution to journal › Article
Mark Gene-centric Association Signals for Lipids and Apolipoproteins Identified via the HumanCVD BeadChip
Talmud, Philippa J. ; Drenos, Fotios ; Shah, Sonia ; Shah, Tina ; Palmen, Jutta ; Verzilli, Claudio ; Gaunt, Tom R. ; Pallas, Jacky ; Lovering, Ruth and Li, Kawah , et al. (2009) In American Journal of Human Genetics 85(5). p.628-642
- Contribution to journal › Article
Mark Folate receptor alpha defect causes cerebral folate transport deficiency: a treatable neurodegenerative disorder associated with disturbed myelin metabolism
Steinfeld, Robert ; Grapp, Marcel ; Kraetzner, Ralph ; Dreha-Kulaczewski, Steffi ; Helms, Gunther ^LU ; Dechent, Peter ; Wevers, Ron ; Grosso, Salvatore and Gaertner, Jutta (2009) In American Journal of Human Genetics 85(3). p.354-363
- Contribution to journal › Article
2008
Mark Independent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk culture
Enattah, Nabil Sabri ; Jensen, Tine G. K. ; Nielsen, Mette ; Lewinski, Rikke ; Kuokkanen, Mikko ; Rasinpera, Heli ; El-Shanti, Hatem ; Seo, Jeong Kee ; Alifrangis, Michael and Khalil, Insaf F. , et al. (2008) In American Journal of Human Genetics 82(1). p.57-72
- Contribution to journal › Article
Mark Identifying Genetic Traces of Historical Expansions : Phoenician Footprints in the Mediterranean
Zalloua, Pierre A. ; Platt, Daniel E. ; El Sibai, Mirvat ; Khalife, Jade ^LU ; Makhoul, Nadine ; Haber, Marc ; Xue, Yali ; Izaabel, Hassan ; Bosch, Elena and Adams, Susan M. , et al. (2008) In American Journal of Human Genetics 83(5). p.633-642
- Contribution to journal › Article
Mark Y-Chromosomal Diversity in Lebanon Is Structured by Recent Historical Events
Zalloua, Pierre A. ; Xue, Yali ; Khalife, Jade ^LU ; Makhoul, Nadine ; Debiane, Labib ; Platt, Daniel E. ; Royyuru, Ajay K. ; Herrera, Rene J. ; Hernanz, David F.Soria and Blue-Smith, Jason , et al. (2008) In American Journal of Human Genetics 82(4). p.873-882
- Contribution to journal › Article
2007
Mark Associating mitochondrial DNA variation with complex traits - Reply to Elson et al.
Saxena, Richa ; de Bakker, Paul I. W. ; Groop, Leif ^LU ; Daly, Mark J. and Altshuler, David (2007) In American Journal of Human Genetics 80(2). p.382-383
- Contribution to journal › Letter
Mark Evidence of still-ongoing convergence evolution of the lactase persistence T-13910 alleles in humans
Enattah, Nabil Sabri ; Trudeau, Aimee ; Pimenoff, Ville ; Maiuri, Luigi ; Auricchio, Salvatore ; Greco, Luigi ; Rossi, Mauro ; Lentze, Michael ; Seo, J. K. and Rahgozar, Soheila , et al. (2007) In American Journal of Human Genetics 81(3). p.615-625
- Contribution to journal › Article
Mark Recurrent 10q22-q23 deletions: a genomic disorder on 10q associated with cognitive and behavioral abnormalities
Balciuniene, Jorune ; Feng, Ningping ; Iyadurai, Kelly ; Hirsch, Betsy ; Charnas, Lawrence ; Bill, Brent R. ; Easterday, Mathew C. ; Staaf, Johan ^LU ; Oseth, LeAnn and Czapansky-Beilman, Desiree , et al. (2007) In American Journal of Human Genetics 80(5). p.938-947
- Contribution to journal › Article

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