string(238) "select * FROM articoli_opac WHERE fonte <> 'ISI' AND fonte='ACNP' AND fasc_anno_pubbl='1985' 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 | 76-100 | >>    

Articles table of contents

Results : 76-100/117
Evidence, Probability, and Paternity.
Authors: Brenner, C. H.
Journal: American journal of human genetics
Citation: H. Brenner, C., Evidence, Probability, and Paternity., American journal of human genetics , 37(4), 1985, pp. 826-826
Chromosomal Imprinting and the Parent Transmission Specific Variation in Expressivity of Huntington Disease.
Authors: Erickson, R. P.
Journal: American journal of human genetics
Citation: P. Erickson, R., Chromosomal Imprinting and the Parent Transmission Specific Variation in Expressivity of Huntington Disease., American journal of human genetics , 37(4), 1985, pp. 827-829
Book Reviews
Authors:
Journal: American journal of human genetics
Citation: , Book Reviews, American journal of human genetics , 37(4), 1985, pp. 830-838
Deletion Mapping of Human Chromosome 5 Using Chromosome-Specific DNA Probes.
Authors: Carlock, L. R. , Skarecky, D. , Dana, S. L. and Wasmuth, J. J.
Journal: American journal of human genetics
Citation: J. Carlock, L. R. , Skarecky, D. , Dana, S. L. And Wasmuth, J., Deletion Mapping of Human Chromosome 5 Using Chromosome-Specific DNA Probes., American journal of human genetics , 37(5), 1985, pp. 839-852
Accurate and Superaccurate Gene Mapping
Authors: Lange, K. , Kunkel, L. , Aldridge, J. and Latt, S. A.
Journal: American journal of human genetics
Citation: A. Lange, K. , Kunkel, L. , Aldridge, J. And Latt, S., Accurate and Superaccurate Gene Mapping, American journal of human genetics , 37(5), 1985, pp. 853-867
Chromosomal Localization of the Human alpha1-Antitrypsin Gene (PI) to 1431-32.
Authors: Schroeder, W. T. , Miller, M. F. , Woo, S. L. C. , and Saunders, G. F.
Journal: American journal of human genetics
Citation: F. Schroeder, W. T. , Miller, M. F. , Woo, S. L. C. , And Saunders, G., Chromosomal Localization of the Human alpha1-Antitrypsin Gene (PI) to 1431-32., American journal of human genetics , 37(5), 1985, pp. 868-872
Chromosomal Localization of the Human Elastin Gene.
Authors: Emanuel, B. S. , Cannizzaro, L. , Ornstein-Goldstein, N. , Indik, Z. K. , Yoon,
Journal: American journal of human genetics
Citation: . Emanuel, B. S. , Cannizzaro, L. , Ornstein-goldstein, N. , Indik, Z. K. , Yoon,, Chromosomal Localization of the Human Elastin Gene., American journal of human genetics , 37(5), 1985, pp. 873-882
The E7-Associated Cell-Surface Antigen: A Marker for the 11p13 Chromosomal Deletion Associated with Aniridia-Wilms Tumor.
Authors: Scoggin, C. H. , Fisher, J. H. , Shoemaker, S. A. , Morse, H. , Leigh, T. , and
Journal: American journal of human genetics
Citation: . Scoggin, C. H. , Fisher, J. H. , Shoemaker, S. A. , Morse, H. , Leigh, T. , And, The E7-Associated Cell-Surface Antigen: A Marker for the 11p13 Chromosomal Deletion Associated with Aniridia-Wilms Tumor., American journal of human genetics , 37(5), 1985, pp. 883-889
Linkage Analysis of a DNA Marker Localized to 20p 12 and Multiple Endocrine Neoplasia Type 2A.
Authors: Goodfellow, P. J. , White, B. N. , Holden, J. J. A. , Duncan, A. M. V. , Sears,
Journal: American journal of human genetics
Citation: . Goodfellow, P. J. , White, B. N. , Holden, J. J. A. , Duncan, A. M. V. , Sears,, Linkage Analysis of a DNA Marker Localized to 20p 12 and Multiple Endocrine Neoplasia Type 2A., American journal of human genetics , 37(5), 1985, pp. 890-897
Twenty-seven Protein Polymorphisms by Two-Dimensional Electrophoresis of Serum, Erythrocytes, and Fibroblasts in Two Pedigrees.
Authors: Goldman, D. , Goldin, L. R. , Rathnagiri, P. , O'Brien, S. J. , Egeland, J. A. a
Journal: American journal of human genetics
Citation: Goldman, D. , Goldin, L. R. , Rathnagiri, P. , O'Brien, S. J. , Egeland, J. A. A, Twenty-seven Protein Polymorphisms by Two-Dimensional Electrophoresis of Serum, Erythrocytes, and Fibroblasts in Two Pedigrees., American journal of human genetics , 37(5), 1985, pp. 898-911
Sandhoff Disease Heterozygote Detection: A Component of Population Screening for Tay-Sachs Disease Carriers. I. Statistical Methods.
Authors: Cantor, R. M. , Lim, J. S. T. , Rov, C. , and Kaback, M. M.
Journal: American journal of human genetics
Citation: M. Cantor, R. M. , Lim, J. S. T. , Rov, C. , And Kaback, M., Sandhoff Disease Heterozygote Detection: A Component of Population Screening for Tay-Sachs Disease Carriers. I. Statistical Methods., American journal of human genetics , 37(5), 1985, pp. 912-921
Improved Resolution of PI (a,-Antitrypsin) Phenotypes by a Large-Scale Immobilized pH Gradient.
Authors: Görg, A. , Postel, W. , Weser, J. , Patutschnick, W. and Cleve, H.
Journal: American journal of human genetics
Citation: H. Görg, A. , Postel, W. , Weser, J. , Patutschnick, W. And Cleve,, Improved Resolution of PI (a,-Antitrypsin) Phenotypes by a Large-Scale Immobilized pH Gradient., American journal of human genetics , 37(5), 1985, pp. 922-930
Normal mRNA Content in a Phosphoglycerate Kinase Variant with Severe Enzyme Deficiency.
Authors: Tani, K. , Takizawa, T. and Yoshida, A.
Journal: American journal of human genetics
Citation: A. Tani, K. , Takizawa, T. And Yoshida,, Normal mRNA Content in a Phosphoglycerate Kinase Variant with Severe Enzyme Deficiency., American journal of human genetics , 37(5), 1985, pp. 931-937
Defective Intramitochondrial NADH Oxidation in Skin Fibroblasts from an Infant with Fetal Neonatal Lacticacidemia.
Authors: Robinson, B. H. , McKay, N. , Goodyer, P. and Lancaster, G.
Journal: American journal of human genetics
Citation: G. Robinson, B. H. , Mckay, N. , Goodyer, P. And Lancaster,, Defective Intramitochondrial NADH Oxidation in Skin Fibroblasts from an Infant with Fetal Neonatal Lacticacidemia., American journal of human genetics , 37(5), 1985, pp. 938-946
Fragile (X) Expression Induced by FUdR Is Transient and Inversely Related to Levels of Thymidylate Synthase Activity.
Authors: Cantú, E. S. , Nussbaum, R. L. , Airhart, S. D. and Ledbetter, D. H.
Journal: American journal of human genetics
Citation: H. Cantú, E. S. , Nussbaum, R. L. , Airhart, S. D. And Ledbetter, D., Fragile (X) Expression Induced by FUdR Is Transient and Inversely Related to Levels of Thymidylate Synthase Activity., American journal of human genetics , 37(5), 1985, pp. 947-955
Unaffected Carrier Males in Families with Fragile X Syndrome.
Authors: Howard-Peebles, P. N. and Friedman, J. M.
Journal: American journal of human genetics
Citation: M. Howard-peebles, P. N. And Friedman, J., Unaffected Carrier Males in Families with Fragile X Syndrome., American journal of human genetics , 37(5), 1985, pp. 956-964
Determination of the Parental Origin of Sex-Chromosome Monosomy Using Restriction Fragment Length Polymorphisms.
Authors: Hassold, T. , Kumlin, E. , Takaesu, N. and Leppert, M.
Journal: American journal of human genetics
Citation: M. Hassold, T. , Kumlin, E. , Takaesu, N. And Leppert,, Determination of the Parental Origin of Sex-Chromosome Monosomy Using Restriction Fragment Length Polymorphisms., American journal of human genetics , 37(5), 1985, pp. 965-972
Differences in the Error Mechanisms Affecting Sex and Autosomal Chromosomes in Women of Different Ages within the Reproductive Age Group.
Authors: Ford, J. H. and Russell, J. A.
Journal: American journal of human genetics
Citation: A. Ford, J. H. And Russell, J., Differences in the Error Mechanisms Affecting Sex and Autosomal Chromosomes in Women of Different Ages within the Reproductive Age Group., American journal of human genetics , 37(5), 1985, pp. 973-983
A Strategy for Using Multiple Linked Markers for Genetic Counseling.
Authors: Chakravarti,A. and Buetow, K. H.
Journal: American journal of human genetics
Citation: H. Chakravarti,a. And Buetow, K., A Strategy for Using Multiple Linked Markers for Genetic Counseling., American journal of human genetics , 37(5), 1985, pp. 984-997
Resolution of Genetic and Cultural Inheritance in Twin Families by Path Analysis: Application to HDL-Cholesterol.
Authors: McGue, M. , Rao, D. C. , Iselius, L. and Russell, J. M.
Journal: American journal of human genetics
Citation: M. Mcgue, M. , Rao, D. C. , Iselius, L. And Russell, J., Resolution of Genetic and Cultural Inheritance in Twin Families by Path Analysis: Application to HDL-Cholesterol., American journal of human genetics , 37(5), 1985, pp. 998-1014
Isolation and Subregional Mapping of an Arbitrary Cloned Probe Detecting a Common RFLP on Human Chromosome 2.
Authors: Davatelis, G. N.
Journal: American journal of human genetics
Citation: N. Davatelis, G., Isolation and Subregional Mapping of an Arbitrary Cloned Probe Detecting a Common RFLP on Human Chromosome 2., American journal of human genetics , 37(5), 1985, pp. 1015-1021
Endogenous Blockage and Delay of the Chromosome Cycle Despite Normal Recruitment and Growth Phase Explain Poor Proliferation and Frequent Endomitosis in Fanconi Anemia Cells.
Authors: Kubbies, M. , Schindler, D. , Hoehn, H. , Schinzel, A. and Rabinovitch, P. S.
Journal: American journal of human genetics
Citation: S. Kubbies, M. , Schindler, D. , Hoehn, H. , Schinzel, A. And Rabinovitch, P., Endogenous Blockage and Delay of the Chromosome Cycle Despite Normal Recruitment and Growth Phase Explain Poor Proliferation and Frequent Endomitosis in Fanconi Anemia Cells., American journal of human genetics , 37(5), 1985, pp. 1022-1030
Frequency of Hexosaminidase A Variant Alleles among Ashkenazi Jews and Prenatal Diagnosis of Gv2 Gangliosidosis.
Authors: Navon, R. and Adam, A.
Journal: American journal of human genetics
Citation: A. Navon, R. And Adam,, Frequency of Hexosaminidase A Variant Alleles among Ashkenazi Jews and Prenatal Diagnosis of Gv2 Gangliosidosis., American journal of human genetics , 37(5), 1985, pp. 1031-1033
Book Reviews
Authors:
Journal: American journal of human genetics
Citation: , Book Reviews, American journal of human genetics , 37(5), 1985, pp. 1034-1048
Nucleolar organizer region variants as a risk factor for down syndrome
Authors: Jackson-Cook, C.K Flannery, D.B. Corey, L.A. Nance, W.E. Brown, J.A.
Journal: American journal of human genetics
Citation: Jackson-cook, C.k et al., Nucleolar organizer region variants as a risk factor for down syndrome, American journal of human genetics , 37(6), 1985, pp. 1049-1061
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