string(238) "select * FROM articoli_opac WHERE fonte <> 'ISI' AND fonte='ACNP' AND fasc_anno_pubbl='1989' AND fasc_issn='00029297' order by level desc, fasc_key desc, NULLIF(regexp_replace(pagina_ini, E'\\D', '', 'g'), '')::int asc offset 25 limit 25" ACNP - Italian Periodicals Catalogue
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Articles table of contents

Results : 26-50/195
Nucleotide variations in the 3' A gamma enhancer region are linked to beta-gene cluster haploytpes and are unrelated to fetal hemoglobin expression
Authors: Ragusa, Angela Lombardo, Mario Bouhassira, Eric Beldjord, Cherif Lombardo, Turridu Nagel, Ronald L. Labie, Dominique Krishnamoorthy, Rajagopal
Journal: American journal of human genetics
Citation: Ragusa, Angela et al., Nucleotide variations in the 3' A gamma enhancer region are linked to beta-gene cluster haploytpes and are unrelated to fetal hemoglobin expression, American journal of human genetics , 45-I(1), 1989, pp. 106-111
A simple method to detect and estimate heterogeneity: application to huntington disease, diabetes, and HIV seroconversion
Authors: Payami, Haydeh
Journal: American journal of human genetics
Citation: Payami, Haydeh, A simple method to detect and estimate heterogeneity: application to huntington disease, diabetes, and HIV seroconversion, American journal of human genetics , 44(1), 1989, pp. 107-114
A new TATA box mutation detected at prenatal diagnosis for beta-thalassemia
Authors: Cai, Shi-Ping Zhang, Ji-Zeng Doherty, Marie Kan, Yuet Wai
Journal: American journal of human genetics
Citation: Cai, Shi-ping et al., A new TATA box mutation detected at prenatal diagnosis for beta-thalassemia, American journal of human genetics , 45-I(1), 1989, pp. 112-114
Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia B
Authors: Ludwig, M. Schwaab, R. Eigel, A. Horst, J. Egli, H. Brackman, H.-H. Olek, K.
Journal: American journal of human genetics
Citation: M. Ludwig, et al., Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia B, American journal of human genetics , 45-I(1), 1989, pp. 115-122
A dicentric recombinant 9 derived from a paracentric inversion: phenotype, cytogenetics, and molecular analysis of centromeres
Authors: Worsham, Maria J. Miller, Dorothy A. Devries, Jeffrey M. Mitchell, Arthur R. Babu, V. Ramesh Suri, V. Weiss, Lester Dyke, Daniel L. :Van
Journal: American journal of human genetics
Citation: J. Worsham, Maria et al., A dicentric recombinant 9 derived from a paracentric inversion: phenotype, cytogenetics, and molecular analysis of centromeres, American journal of human genetics , 44(1), 1989, pp. 115-123
Ornithine transcarbamylase deficiency resulting from a C-to-T substitution in exon 5 of the ornithine transcarbamylase gene
Authors: Hata, Akira Setoyama, Chiaki Shimada, Kazunori Takeda, Eiji Kuroda, Yasuhiro Akaboshi, Izumi Matsuda, Ichiro
Journal: American journal of human genetics
Citation: Hata, Akira et al., Ornithine transcarbamylase deficiency resulting from a C-to-T substitution in exon 5 of the ornithine transcarbamylase gene, American journal of human genetics , 45-I(1), 1989, pp. 123-127
Genetic determination of plasma apolipoprotein AI in a population-based sample
Authors: Moll, Patricia P. Michels, Virginia V. Weidman, William H. Kottke, Bruce A.
Journal: American journal of human genetics
Citation: P. Moll, Patricia et al., Genetic determination of plasma apolipoprotein AI in a population-based sample, American journal of human genetics , 44(1), 1989, pp. 124-139
Comparative mapping of the constitutional and tumor associated 11;22 translocations
Authors: Budart, Marcia Sellinger, Beatrice Griffin, Constance Emanuel, Beverly S.
Journal: American journal of human genetics
Citation: Budart, Marcia et al., Comparative mapping of the constitutional and tumor associated 11;22 translocations, American journal of human genetics , 45-I(1), 1989, pp. 128-139
Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a french-canadian population
Authors: MacKenzie, A. E. MacLeod, H. L. W. Hunter, A. G. Korneluk, R. G.
Journal: American journal of human genetics
Citation: E. Mackenzie, A. et al., Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a french-canadian population, American journal of human genetics , 44(1), 1989, pp. 140-147
Hypopigmentation: a common feature of prader-labhart-willi syndrome
Authors: Merlin G. Butler
Journal: American journal of human genetics
Citation: Merlin G. Butler, Hypopigmentation: a common feature of prader-labhart-willi syndrome, American journal of human genetics , 45-I(1), 1989, pp. 140-146
Genetic studies of human apolipoproteins. IX. apolipoprotein D polymorphism and its relation to serum lipoprotein lipid levels
Authors: Kamboh, M. I. Albers, I. I. Majumder, P. P. Ferrell, R. E.
Journal: American journal of human genetics
Citation: I. Kamboh, M. et al., Genetic studies of human apolipoproteins. IX. apolipoprotein D polymorphism and its relation to serum lipoprotein lipid levels, American journal of human genetics , 45-I(1), 1989, pp. 147-154
Genetic studies of low-abundance human plasma proteins. XIll. population genetics of the CIR complement subcomponent and description of new variants
Authors: Kamboh, M. I. Lyons, L. A. Ferrell, R. E.
Journal: American journal of human genetics
Citation: I. Kamboh, M. et al., Genetic studies of low-abundance human plasma proteins. XIll. population genetics of the CIR complement subcomponent and description of new variants, American journal of human genetics , 44(1), 1989, pp. 148-153
Human population genetic studies of five hypervariable DNA loci
Authors: Balazs, Ivan Baird, Michael Clyne, Mindy Meade, Ellie
Journal: American journal of human genetics
Citation: Balazs, Ivan et al., Human population genetic studies of five hypervariable DNA loci, American journal of human genetics , 44(2), 1989, pp. 182-190
On the possibility of pleiotropic monogenic control of hereditary polyposis and primary cancer of colon
Authors: Ginsburg, E. Kh. Axenovich, T. I. Altshouler, B. A. Bazhenova, M. D.
Journal: American journal of human genetics
Citation: Ginsburg, E. Kh et al., On the possibility of pleiotropic monogenic control of hereditary polyposis and primary cancer of colon, American journal of human genetics , 44(2), 1989, pp. 191-197
Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism
Authors: Thomas, loan T. Frias, Jaime L. Cantu, Eduardo S. Lafer, Charlotte Z. Flannery, David B. Graham, John G. jr. ,
Journal: American journal of human genetics
Citation: T. Thomas, Loan et al., Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism, American journal of human genetics , 45-I(2), 1989, pp. 193-205
Galactocerebrosidase activity in somatic cell hybrids derived from twitcher mouse/control human fibroblasts is associated with human chromosme 17
Authors: Lyerla, Timothy A. Konola, Jukka T. Skiba, Mark C. Raghavan, Srinivasa
Journal: American journal of human genetics
Citation: A. Lyerla, Timothy et al., Galactocerebrosidase activity in somatic cell hybrids derived from twitcher mouse/control human fibroblasts is associated with human chromosme 17, American journal of human genetics , 44(2), 1989, pp. 198-207
Genetic heterogeneity in leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism
Authors: Vilkki, Johanna Savontaus, Marja-Liisa Nikoskelainen, Eeva K.
Journal: American journal of human genetics
Citation: Vilkki, Johanna et al., Genetic heterogeneity in leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism, American journal of human genetics , 45-I(2), 1989, pp. 206-211
The clinical and screening age-at-onset distribution for the men-2 syndrome
Authors: Easton, D. F. Ponder, M. A. Cummings, T. Gagel, R. F. Hansen, H. H. Reichlin, S. Tashjian, A. H. Jr., Telenius-Berg, M. Ponder, B. A. J. the Cancer Research Campaign Medullary Thyroid Group
Journal: American journal of human genetics
Citation: F. Easton, D. et al., The clinical and screening age-at-onset distribution for the men-2 syndrome, American journal of human genetics , 44(2), 1989, pp. 208-215
Gaucher disease: molecular heterogeneity and phenotype-genotype correlations
Authors: Theophilus, Bimal Latham, Theresa Grabowski, Gregory A. Smith, Frances I.
Journal: American journal of human genetics
Citation: Theophilus, Bimal et al., Gaucher disease: molecular heterogeneity and phenotype-genotype correlations, American journal of human genetics , 45-I(2), 1989, pp. 212-225
Identifying pedigrees segregating at a major locus for a quantitative trait: an efficient strategy for linkage analysis
Authors: Boehnke, Michael P. Moll, Patricia
Journal: American journal of human genetics
Citation: Boehnke, Michael et P. Moll, Patricia, Identifying pedigrees segregating at a major locus for a quantitative trait: an efficient strategy for linkage analysis, American journal of human genetics , 44(2), 1989, pp. 216-224
Spina bifida and hydrocephalus: a population study over a 35-year period
Authors: Bamforth, Stephen J. Baird, Patricia A.
Journal: American journal of human genetics
Citation: J. Bamforth, Stephen et A. Baird, Patricia, Spina bifida and hydrocephalus: a population study over a 35-year period, American journal of human genetics , 44(2), 1989, pp. 225-232
Analyzing the relationship between age at onset and risk to relatives
Authors: Neale, Michael C. Eaves, Lindon J. Hewitt, John K. MacLean, Charles J. Meyer, Joanne M. Kendler, Kenneth S.
Journal: American journal of human genetics
Citation: C. Neale, Michael et al., Analyzing the relationship between age at onset and risk to relatives, American journal of human genetics , 45-I(2), 1989, pp. 226-239
Two point mutations are responsible for g6pd polymorphism in sardinia
Authors: De Vita, Gabriella Alcalay, Myriam Sampietro, Maurizio Cappellini, M. Domenica Fiorelli, Gemino Toniolo, Daniela
Journal: American journal of human genetics
Citation: De Vita, Gabriella et al., Two point mutations are responsible for g6pd polymorphism in sardinia, American journal of human genetics , 44(2), 1989, pp. 233-240
Cardiovascular risk factors in a french-canadian population: resolution of genetic and familial environmental effects on blood pressure by using extensive information on environmental correlates
Authors: Pérusse, Louis Rice, Treva Bouchard, Claude Vogler, George P. Rao, D. C.
Journal: American journal of human genetics
Citation: Pérusse, Louis et al., Cardiovascular risk factors in a french-canadian population: resolution of genetic and familial environmental effects on blood pressure by using extensive information on environmental correlates, American journal of human genetics , 45-I(2), 1989, pp. 240-251
Lowe oculocerebrorenal syndrome: dna-based linkage of the gene to xq24-q26, using tightly linked flanking markers and the correlation to lens examination in carrier diagnosis
Authors: Wadelius, Claes Fagerholm, Per Pettersson, Ulf Annerén, Göran
Journal: American journal of human genetics
Citation: Wadelius, Claes et al., Lowe oculocerebrorenal syndrome: dna-based linkage of the gene to xq24-q26, using tightly linked flanking markers and the correlation to lens examination in carrier diagnosis, American journal of human genetics , 44(2), 1989, pp. 241-247
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