string(238) "select * FROM articoli_opac WHERE fonte <> 'ISI' AND fonte='ACNP' AND fasc_anno_pubbl='2003' AND fasc_issn='00029297' order by level desc, fasc_key desc, NULLIF(regexp_replace(pagina_ini, E'\\D', '', 'g'), '')::int asc offset 50 limit 25" ACNP - Italian Periodicals Catalogue
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Articles table of contents

Results : 51-75/181
Estimation of Haplotype Frequencies, Linkage-Disequilibrium Measures, and Combination of Haplotype Copies in Each Pool by Use of Pooled DNA Data
Authors: Ito, Toshikazu Chiku, Suenori Inoue, Eisuke Tomita, Makoto Morisaki, Takayuki Morisaki, Hiroko Kamatani, Naoyuki
Journal: American journal of human genetics
Citation: Ito, Toshikazu et al., Estimation of Haplotype Frequencies, Linkage-Disequilibrium Measures, and Combination of Haplotype Copies in Each Pool by Use of Pooled DNA Data, American journal of human genetics , 72(2), 2003, pp. 384-398
Skewed X-Chromosome Inactivation Is Associated with Trisomy in Women Ascertained on the Basis of Recurrent Spontaneous Abortion or Chromosomally Abnormal Pregnancies
Authors: Beever, C.L. Stephenson, M.D. Peñaherrera, M.S. Jiang, R.H. Kalousek, D.K. Hayden, M. Field, L. Brown, C.J. Robinson, W.P.
Journal: American journal of human genetics
Citation: Beever, C.l et al., Skewed X-Chromosome Inactivation Is Associated with Trisomy in Women Ascertained on the Basis of Recurrent Spontaneous Abortion or Chromosomally Abnormal Pregnancies, American journal of human genetics , 72(2), 2003, pp. 399-407
Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia
Authors: Paznekas, William Boyadjiev, Simeon A. Shapiro, Robert E. Daniels, Otto Wollnik, Bernd Keegan, Catherine E. Innis, Jeffrey W. Dinulos, Mary Beth Christian, Cathy Hannibal, Mark C. Wang Jabs, Ethylin
Journal: American journal of human genetics
Citation: Paznekas, William et al., Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia, American journal of human genetics , 72(2), 2003, pp. 408-418
Mental Retardation and Abnormal Skeletal Development (Dyggve-Melchior-Clausen Dysplasia) Due to Mutations in a Novel, Evolutionarily Conserved Gene
Authors: Cohn, Daniel H. Ehtesham, Nadia Krakow, Deborah Unger, Sheila Shanske, Alan Reinker, Kent Powell, Berkley R. Rimoin, David L.
Journal: American journal of human genetics
Citation: H. Cohn, Daniel et al., Mental Retardation and Abnormal Skeletal Development (Dyggve-Melchior-Clausen Dysplasia) Due to Mutations in a Novel, Evolutionarily Conserved Gene, American journal of human genetics , 72(2), 2003, pp. 419-428
Evaluation of Complex Inheritance Involving the Most Common Bardet-Biedl Syndrome Locus (BBS1)
Authors: Mykytyn, Kirk Nishimura, Darryl Y. Searby, Charles C. Beck, Gretel Bugge, Kevin Haines, Heidi L. Cornier, Alberto S. Cox, Gerald F. Fulton, Anne B. Carmi, Rivka Iannaccone, Alessandro Jacobson, Samuel G. Weleber, Richard G. Wright, Alan F. Riise, Ruth Hennekam, C.M. Raoul Lüleci, Güven Berker-Karauzum, Sibel Biesecker, Leslie G. Stone, Edwin M. Sheffield, Val C.
Journal: American journal of human genetics
Citation: Mykytyn, Kirk et al., Evaluation of Complex Inheritance Involving the Most Common Bardet-Biedl Syndrome Locus (BBS1), American journal of human genetics , 72(2), 2003, pp. 429-437
Studying Parents and Grandparents to Assess Genetic Contributions to Early-Onset Disease
Authors: Weinberg, Clarice R.
Journal: American journal of human genetics
Citation: R. Weinberg, Clarice, Studying Parents and Grandparents to Assess Genetic Contributions to Early-Onset Disease, American journal of human genetics , 72(2), 2003, pp. 438-447
Genomewide Linkage Analysis Identifies Polymorphism in the Human Interferon-. Receptor Affecting Helicobacter pylori Infection
Authors: Thye, Thorsten Bruchard, Gerd D. Nilius, Manfred Müller-Myhsok, Bertram Horstmann, Rolf D.
Journal: American journal of human genetics
Citation: Thye, Thorsten et al., Genomewide Linkage Analysis Identifies Polymorphism in the Human Interferon-. Receptor Affecting Helicobacter pylori Infection, American journal of human genetics , 72(2), 2003, pp. 448-453
Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate Alleles
Authors: Nolin, Sarah L Brown, W. Ted Glicksman, Anne Houck, George E., Jr. Gargano, Alice D. Sullivan, Amy Biancalana, Valérie Bröndum-Nielsen, Karen Hjalgrim, Helle Holinski-Feder, Elke Kooy, Frank Longshore, John Macpherson, James Mandel, Jean-Louis Matthijs, Geert Rousseau, Francois Steinbach, Peter Väisänen, Marja-Leena von Koskull, Harriet Sherman, Stephanie L.
Journal: American journal of human genetics
Citation: L. Nolin, Sarah et al., Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate Alleles, American journal of human genetics , 72(2), 2003, pp. 454-464
Natural Selection on the Olfactory Receptor Gene Family in Humans and Chimpanzees
Authors: Gilad, Yoav Bustamante, Carlos D. Lancet, Doron Pääbo, Svante
Journal: American journal of human genetics
Citation: Gilad, Yoav et al., Natural Selection on the Olfactory Receptor Gene Family in Humans and Chimpanzees, American journal of human genetics , 73(3), 2003, pp. 489-501
Assessing the Performance of the Haplotype Block Model of Linkage Disequilibrium
Authors: Wall, Jeffrey D. Pritchard, Jonathan K.
Journal: American journal of human genetics
Citation: D. Wall, Jeffrey et K. Pritchard, Jonathan, Assessing the Performance of the Haplotype Block Model of Linkage Disequilibrium, American journal of human genetics , 73(3), 2003, pp. 502-515
A Novel NOD2/CARD15 Haplotype Conferring Risk for Crohn Disease in Ashkenazi Jews
Authors: Sugimura, Kazuhito Taylor, Kent D. Lin, Ying-chao Hang, Tieu Wang, Dai Tang, Yong-Ming Fischel-Ghodsian, Nathan Targan, Stephan R. Rotter, Jerome I. Yang, Huiying
Journal: American journal of human genetics
Citation: Sugimura, Kazuhito et al., A Novel NOD2/CARD15 Haplotype Conferring Risk for Crohn Disease in Ashkenazi Jews, American journal of human genetics , 72(3), 2003, pp. 509-518
Estimation of the Inbreeding Coefficient through Use of Genomic Data
Authors: Leutnegger, Anne-Louise Prum, Bernard Génin, Emmanuelle Verny, Christophe Lemainque, Arnaud Clerget-Darpoux, Françoise Thompson, Elizabeth A.
Journal: American journal of human genetics
Citation: Leutnegger, Anne-louise et al., Estimation of the Inbreeding Coefficient through Use of Genomic Data, American journal of human genetics , 73(3), 2003, pp. 516-523
Reciprocal and Nonreciprocal Recombination at the Glucocerebrosidase Gene Region: Implications for Complexity in Gaucher Disease
Authors: Tayebi, Nahid Stubblefield, Barbara K. Park, Joseph K. Orvisky, Eduard Walker, Jamie M. LaMarca, Mary E. Sidransky, Ellen
Journal: American journal of human genetics
Citation: Tayebi, Nahid et al., Reciprocal and Nonreciprocal Recombination at the Glucocerebrosidase Gene Region: Implications for Complexity in Gaucher Disease, American journal of human genetics , 72(3), 2003, pp. 519-534
Y-Chromosome Evidence for Differing Ancient Demographic Histories in the Americas
Authors: Bortolini, Maria-Catira Salzano, Francisco M. Thomas, Mark G. Stuart, Steven Nasenen, Selja P.K. Bau, Claiton H.D. Hutz, Mara H. Layrisse, Zulay Petzl-Erler, Maria L. Tsuneto, Luiza T. Hill, Kim Hurtado, Ana M. Castro-de-Guerra, Dinorah Torres, Maria M. Groot, Helena Michalski, Roman Nymadawa, Pagbajabyn Bedoya, Gabriel Bradman, Neil Labuda, Damian Ruiz-Linares, Andres
Journal: American journal of human genetics
Citation: Bortolini, Maria-catira et al., Y-Chromosome Evidence for Differing Ancient Demographic Histories in the Americas, American journal of human genetics , 73(3), 2003, pp. 524-539
Failure to Find DUP25 in Patients with Anxiety Disorders, in Control Individuals, or in Previously Reported Positive Control Cell Lines
Authors: Tabiner, Melody Youings, Sheila Dennis, Nicholas Baldwin, David Buis, Christel Mayers, Andrew Jacobs, Patricia A. Crolla, John A.
Journal: American journal of human genetics
Citation: Tabiner, Melody et al., Failure to Find DUP25 in Patients with Anxiety Disorders, in Control Individuals, or in Previously Reported Positive Control Cell Lines, American journal of human genetics , 72(3), 2003, pp. 535-538
Fine Mapping of Autistic Disorder to Chromosome 15q11-q13 by Use of Phenotypic Subtypes
Authors: Shao, Yujun Cuccaro, M.L. Hauser, E.R. Raiford, K.L. Menold, M.M. Wolpert, C.M. Ravan, S.A. Elston, L. Decena, K. Donnelly, S.L. Abramson, R.K. Wright, H.H. DeLong, G.R. Gilbert, J.R. Pericak-Vance, M.A.
Journal: American journal of human genetics
Citation: Shao, Yujun et al., Fine Mapping of Autistic Disorder to Chromosome 15q11-q13 by Use of Phenotypic Subtypes, American journal of human genetics , 72(3), 2003, pp. 539-548
Age-Related Macular Degeneration.a Genome Scan in Extended Families
Authors: Majewski, Jacek Schultz, Dennis W. Welber, Richard G. Schain, Mitchell B. Edwards, Albert O. Matise, Tara C. Acott, Ted S. Ott, Jurg Klein, Michael L.
Journal: American journal of human genetics
Citation: Majewski, Jacek et al., Age-Related Macular Degeneration.a Genome Scan in Extended Families, American journal of human genetics , 73(3), 2003, pp. 540-550
Accumulation of Mitochondrial DNA Mutations in Human Immunodeficiency Virus.Infected Patients Treated with Nucleoside-Analogue Reverse-Transcriptase Inhibitors
Authors: Martin, Annalise, M. Hammond, Emma Nolan, David Pace, Craig Den Boer, Marion Taylor, Louise Moore, Hannah Martinez, Olga Patricia Christiansen, Frank T. Mallal, Simon
Journal: American journal of human genetics
Citation: M. Martin, Annalise, et al., Accumulation of Mitochondrial DNA Mutations in Human Immunodeficiency Virus.Infected Patients Treated with Nucleoside-Analogue Reverse-Transcriptase Inhibitors, American journal of human genetics , 72(3), 2003, pp. 549-560
Selection and Evaluation of Tagging SNPs in the Neuronal-Sodium-Channel Gene SCN1A: Implications for Linkage-Disequilibrium Gene Mapping
Authors: Waele, Mike E. Depondt, Chantal Macdonald, Stuart J. Smith, Alice Lai, Poh San Shorvon, Simon D. Wood, Nicholas W. Goldstein, David B.
Journal: American journal of human genetics
Citation: E. Waele, Mike et al., Selection and Evaluation of Tagging SNPs in the Neuronal-Sodium-Channel Gene SCN1A: Implications for Linkage-Disequilibrium Gene Mapping, American journal of human genetics , 73(3), 2003, pp. 551-565
Use of Multivariate Linkage Analysis for Dissection of a Complex Cognitive Trait
Authors: Marlow, Angela J. Fisher, Simonn E. Francks, Clyde MacPhie, L. Laurence Cherny, Stacey S. Richardson, Alex J. Talcott, Joel B. Stein, John F. Monaco Anthony P. Cardon, Lon R.
Journal: American journal of human genetics
Citation: J. Marlow, Angela et al., Use of Multivariate Linkage Analysis for Dissection of a Complex Cognitive Trait, American journal of human genetics , 72(3), 2003, pp. 561-570
Transmission/Disequilibrium Test Based on Haplotype Sharing for Tightly Linked Markers
Authors: Zhang, Shuanglin Sha, Qiuying Chen, Huann-Sheng Dong, Jianping Jiang, Renfang
Journal: American journal of human genetics
Citation: Zhang, Shuanglin et al., Transmission/Disequilibrium Test Based on Haplotype Sharing for Tightly Linked Markers, American journal of human genetics , 73(3), 2003, pp. 566-579
Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect
Authors: Buiting, Karin Groß, Stephanie Lich, Christina Gillessen-Kaesbach, Gabriele El-Maarri, Osman Horsthemke, Bernhard
Journal: American journal of human genetics
Citation: Buiting, Karin et al., Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect, American journal of human genetics , 72(3), 2003, pp. 571-577
Human Population Genetic Structure and Inference of Group Membership
Authors: Bamshad, Michael J. Wooding, Stephen Watkins, W. Scott Ostler, Christopher T. Batzer, Mark A. Jorde, Lynn B.
Journal: American journal of human genetics
Citation: J. Bamshad, Michael et al., Human Population Genetic Structure and Inference of Group Membership, American journal of human genetics , 72(3), 2003, pp. 578-589
An Integrated Haplotype Map of the Human Major Histocompatibility Complex
Authors: Walsh, Emily C. Mather, Kristie A. Schaffner, Stephen F. Farwell, Lisa Daly, Mark J. Patterson, Nick Cullen, Michael Carrington, Mary Bugawan, Teodorica L. Erlich, Henry Campbell, Jay Barrett, Jeffrey Miller, Katie Thomson, Glenys Lander, Eric S. Rioux, John D.
Journal: American journal of human genetics
Citation: C. Walsh, Emily et al., An Integrated Haplotype Map of the Human Major Histocompatibility Complex, American journal of human genetics , 73(3), 2003, pp. 580-590
Mapping the Wolf-Hirschhorn Syndrome Phenotype Outside the Currently Accepted WHS Critical Region and Defining a New Critical Region, WHSCR-2
Authors: Zollino, Marcello Lecce, Rossetta Fischetto, Rita Murdolo, Marina Favarelli, Francesca Selicorni, Angelo Buttè, Cinzia Memo, Luigi Capovilla, Giuseppe Neri, Giovanni
Journal: American journal of human genetics
Citation: Zollino, Marcello et al., Mapping the Wolf-Hirschhorn Syndrome Phenotype Outside the Currently Accepted WHS Critical Region and Defining a New Critical Region, WHSCR-2, American journal of human genetics , 72(3), 2003, pp. 590-597
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