string(238) "select * FROM articoli_opac WHERE fonte <> 'ISI' AND fonte='ACNP' AND fasc_anno_pubbl='2002' AND fasc_issn='00029297' order by level desc, fasc_key desc, NULLIF(regexp_replace(pagina_ini, E'\\D', '', 'g'), '')::int asc offset 75 limit 25" ACNP - Italian Periodicals Catalogue
Results: 1-25 | 26-50 | 51-75 | 76-85    

Articles table of contents

Results : 76-85/85
Evidence That Paternal Expression of the .-Sarcoglycan Gene Accounts for Reduced Penetrance in Myoclonus-Dystonia
Authors: Müller, Birgitt Hedrich, Katja Kock, Norman Dragasevic, Natasa Svetel, Marina Garrels, Jennifer Landt, Olfert Nitschke, Matthias Pramstaller, Peter P. Reik, Wolf Schwinger, Eberhard Sperner, Jürgen Ozelius, Laurie Kostic, Vladimir Klein, Christine
Journal: American journal of human genetics
Citation: Müller, Birgitt et al., Evidence That Paternal Expression of the .-Sarcoglycan Gene Accounts for Reduced Penetrance in Myoclonus-Dystonia, American journal of human genetics , 71(6), 2002, pp. 1303-1311
RHD Maternal-Fetal Genotype Incompatibility Increases Schizophrenia Susceptibility
Authors: Palmer, Christina G.S. Turunen, Joni A. Sinsheimer, Janet S. Minassian, Sonia Paunio, Tiina Lönnqvist, Jouko Peltonen, Leena Woodward, J. Arthur
Journal: American journal of human genetics
Citation: Palmer, Christina G.s et al., RHD Maternal-Fetal Genotype Incompatibility Increases Schizophrenia Susceptibility, American journal of human genetics , 71(6), 2002, pp. 1312-1319
Molecular Analysis of Collagen XVIII Reveals Novel Mutations, Presence of a Third Isoform, and Possible Genetic Heterogeneity in Knobloch Syndrome
Authors: Suzuki, O.T. Sertié, A.L. Der Kaloustan, V.M. Kok, F. Carpenter, M. Murray, J. Czeizel, A.E. Kliemann, S.E. Rosemberg, S. Monteiro, M. Olsen, B.R. Passos-Bueno, M.R.
Journal: American journal of human genetics
Citation: Suzuki, O.t et al., Molecular Analysis of Collagen XVIII Reveals Novel Mutations, Presence of a Third Isoform, and Possible Genetic Heterogeneity in Knobloch Syndrome, American journal of human genetics , 71(6), 2002, pp. 1320-1329
Power and Design Considerations for a General Class of Family-Based Association Tests: Quantitative Traits
Authors: Lange, Christoph DeMeo, Dawn L. Laird, Nan M.
Journal: American journal of human genetics
Citation: Lange, Christoph et al., Power and Design Considerations for a General Class of Family-Based Association Tests: Quantitative Traits, American journal of human genetics , 71(6), 2002, pp. 1330-1341
Direct Detection of Insertion/Deletion Polymorphisms in an Autosomal Region by Analyzing High-Density Markers in Individual Spermatozoa
Authors: Pramanik, Sreemanta Li, Honghua
Journal: American journal of human genetics
Citation: Pramanik, Sreemanta et Li, Honghua, Direct Detection of Insertion/Deletion Polymorphisms in an Autosomal Region by Analyzing High-Density Markers in Individual Spermatozoa, American journal of human genetics , 71(6), 2002, pp. 1342-1352
Male Mouse Recombination Maps for Each Autosome Identified by Chromosome Painting
Authors: Froenicke, Lutz Anderson, Lorinda K. Wienberg, Johannes Ashley, Terry
Journal: American journal of human genetics
Citation: Froenicke, Lutz et al., Male Mouse Recombination Maps for Each Autosome Identified by Chromosome Painting, American journal of human genetics , 71(6), 2002, pp. 1353-1368
Multiplex Relative Risk and Estimation of the Number of Loci Underlying an Inherited Disease
Authors: Schliekelman, Paul Slatkin, Montgomery
Journal: American journal of human genetics
Citation: Schliekelman, Paul et Slatkin, Montgomery, Multiplex Relative Risk and Estimation of the Number of Loci Underlying an Inherited Disease, American journal of human genetics , 71(6), 2002, pp. 1369-1385
Haplotype Block Structure and Its Applications to Association Studies: Power and Study Designs
Authors: Zhang, Kui Calabrese, Peter Nordborg, Magnus Sun, Fengzhu
Journal: American journal of human genetics
Citation: Zhang, Kui et al., Haplotype Block Structure and Its Applications to Association Studies: Power and Study Designs, American journal of human genetics , 71(6), 2002, pp. 1386-1394
The Founder Mutation MSH21906G.C Is an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Ashkenazi Jewish Population
Authors: Foulkes, W.D. Thiffault, I. Gruber, S.B. Horwitz, M. Hamel, N. Lee, C. Shia, J. Markowitz, A. Figer, A. Friedman, E. Farber, D. Greenwood, C.M.T. Bonner, J.D. Nafa, K. Walsh, T. Marcus, V. Tomsho, L. Gebert, J. Macrae, F.A. Gaff. C.L. Bressac-de Paillerets, B. Gregersen, P.K. Weitzel, J.N. Gordon, P.H. MacNamara, E. King, M.-C. Hampel, H. de la Chapelle, A. Boyd, J. Offit, K. Rennert, G. Chong, G. Ellis, N.A.
Journal: American journal of human genetics
Citation: Foulkes, W.d et al., The Founder Mutation MSH21906G.C Is an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Ashkenazi Jewish Population, American journal of human genetics , 71(6), 2002, pp. 1395-1412
The Demographics and Distribution of Type B Niemann-Pick Disease: Novel Mutations Lead to New Genotype/Phenotype Correlations
Authors: Simonaro, Calogera M. Desnick, Robert J. McGovern, Margaret M. Wasserstein, Melissa P. Schuchman, Edward H.
Journal: American journal of human genetics
Citation: M. Simonaro, Calogera et al., The Demographics and Distribution of Type B Niemann-Pick Disease: Novel Mutations Lead to New Genotype/Phenotype Correlations, American journal of human genetics , 71(6), 2002, pp. 1413-1419
Results: 1-25 | 26-50 | 51-75 | 76-85