string(238) "select * FROM articoli_opac WHERE fonte <> 'ISI' AND fonte='ACNP' AND fasc_anno_pubbl='1987' 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
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Articles table of contents

Results : 76-100/119
Prenatal diagnosis of sickle hemoglobinopathies: the experience of the columbia university comprehensive center for sickle cell disease
Authors: Driscoll, M.C. Lerner, N. Anyane-Yeboa, K. Maidman, J. Warburton, D. Schaefer-Rego, K. Hsu, R. Ince, C. Malin, J. Pallai, M. Mears, J.G. Bank, A.
Journal: American journal of human genetics
Citation: Driscoll, M.c et al., Prenatal diagnosis of sickle hemoglobinopathies: the experience of the columbia university comprehensive center for sickle cell disease, American journal of human genetics , 40(6), 1987, pp. 548-558
The economics of clinical genetics services I. preview
Authors: Pyeritz, Reed E. Tumpson, Jane E. Bernhardt, Barbara A.
Journal: American journal of human genetics
Citation: E. Pyeritz, Reed et al., The economics of clinical genetics services I. preview, American journal of human genetics , 41-II(4), 1987, pp. 549-558
The economies II. A time of clinical genetics services analysis of a medical genetics clinic
Authors: Bernhardt, Barbara A. Weiner, Janet Foster, Ella C. Tumpson, Jane E. Pyeritz, Reed E.
Journal: American journal of human genetics
Citation: A. Bernhardt, Barbara et al., The economies II. A time of clinical genetics services analysis of a medical genetics clinic, American journal of human genetics , 41-II(4), 1987, pp. 559-565
Association of congenital deficiency of multiple vitamin k-dependent coagulation factors and the phenotype of the warfarin embryopathy: clues to the mechanism of teratogenicity of coumarin derivatives
Authors: Pauli, Richard M. Lian, Jane B. Mosher, Deane F. Suttie, John W.
Journal: American journal of human genetics
Citation: M. Pauli, Richard et al., Association of congenital deficiency of multiple vitamin k-dependent coagulation factors and the phenotype of the warfarin embryopathy: clues to the mechanism of teratogenicity of coumarin derivatives, American journal of human genetics , 41-II(4), 1987, pp. 566-583
Abnormal kinetic behavior of cytochrome oxidase in a case of leigh disease
Authors: Glerum, Moira Robinson, Brian H. Spratt, Clifford Wilson, John Patrick, Desmond
Journal: American journal of human genetics
Citation: Glerum, Moira et al., Abnormal kinetic behavior of cytochrome oxidase in a case of leigh disease, American journal of human genetics , 41-II(4), 1987, pp. 584-593
An XXX male resulting from paternal X-Y interchange and maternai X-X non- disjunction
Authors: Annerén, Goran Andersson, Mea Page, David C. Brown, Laura G. Berg, Matts Läck- gren, Goran Gustavson, Karl-Henrik De la Chapelle, Albert
Journal: American journal of human genetics
Citation: Annerén, Goran et al., An XXX male resulting from paternal X-Y interchange and maternai X-X non- disjunction, American journal of human genetics , 41-II(4), 1987, pp. 594-604
Isolation of a cDNA clone for the human laminin-B1 chain and its gene localization
Authors: Jaye, Micheal Modi, William S. Ricca, George A. Mudd, Robert Chiu, Ing-Ming O'Brien, Stephen J. Drohan, William N.
Journal: American journal of human genetics
Citation: Jaye, Micheal et al., Isolation of a cDNA clone for the human laminin-B1 chain and its gene localization, American journal of human genetics , 41-II(4), 1987, pp. 605-615
The gene encoding human vimentin is located on the short arm of chromosome 10
Authors: Ferrari, Sergio Cannizzaro, Linda A. Battini, Renata Huebner, Kay Baserga, Renato
Journal: American journal of human genetics
Citation: Ferrari, Sergio et al., The gene encoding human vimentin is located on the short arm of chromosome 10, American journal of human genetics , 41-II(4), 1987, pp. 616-626
Linkage studies of friedreich ataxia by means of blood-group and protein markers
Authors: Keats, B. J. B. Ward, L. J. Krieger, M. Lu, S. Wilensky, M. A. Forster- Gibson, C. J. Roy, M. Monté, M. Barbeau, A. Simpson, N. E. Eiberg, H. Tippett, P. Williamson, R. Chamberlain, S.
Journal: American journal of human genetics
Citation: B. Keats, B. J. et al., Linkage studies of friedreich ataxia by means of blood-group and protein markers, American journal of human genetics , 41-II(4), 1987, pp. 627-634
Linkage relationships between X-linked retinitis pigmentosa and six short arm markers: exclusion of the disease locus from Xp21 and localization to be- tween DXS7 and DXS14
Authors: Wright, Alan F. Bhattacharya, Shom S. Clayton, John F. Dempster, Maureen Tippett, Patricia McKeown, Carole M. E. Jay, Marcelle Jay, Barrie Bird, Alan C.
Journal: American journal of human genetics
Citation: F. Wright, Alan et al., Linkage relationships between X-linked retinitis pigmentosa and six short arm markers: exclusion of the disease locus from Xp21 and localization to be- tween DXS7 and DXS14, American journal of human genetics , 41-II(4), 1987, pp. 635-644
Genetic studies of low-abundance human plasma proteins. V. polymorphism of hemopexin
Authors: Kamboh, M. I. Ferrell, R. E.
Journal: American journal of human genetics
Citation: I. Kamboh, M. et E. Ferrell, R., Genetic studies of low-abundance human plasma proteins. V. polymorphism of hemopexin, American journal of human genetics , 41-II(4), 1987, pp. 645-653
Human ferritin genes: chromosomal assignments and polymorphisms
Authors: Garti, Richard A. Shaked, Roy Mohandas, T. K. Salser, Winston
Journal: American journal of human genetics
Citation: A. Garti, Richard et al., Human ferritin genes: chromosomal assignments and polymorphisms, American journal of human genetics , 41-II(4), 1987, pp. 654-667
Rapid karyotyping of neonates on the basis of data from cord blood
Authors: Garnham, Ian Sutherland, Grant R.
Journal: American journal of human genetics
Citation: Garnham, Ian et R. Sutherland, Grant, Rapid karyotyping of neonates on the basis of data from cord blood, American journal of human genetics , 41-II(4), 1987, pp. 668-670
The effects thai retessioreening and assortative maring on lethal recessive-allele frequencies and homozygote incidence
Authors: Campbell, R. B.
Journal: American journal of human genetics
Citation: B. Campbell, R., The effects thai retessioreening and assortative maring on lethal recessive-allele frequencies and homozygote incidence, American journal of human genetics , 41-II(4), 1987, pp. 671-677
Distribution of 3-thalassemia mutations in south china and their association with haplotypes
Authors: Chan, Vivian Chan, T. K. Chebab, F. F. Todd, D.
Journal: American journal of human genetics
Citation: Chan, Vivian et al., Distribution of 3-thalassemia mutations in south china and their association with haplotypes, American journal of human genetics , 41-II(4), 1987, pp. 678-685
A controlled study of tourette syndrome. I. attention-deficit disorder, learning disorders, and school problems
Authors: Comings, David E. Comings, Brenda G.
Journal: American journal of human genetics
Citation: E. Comings, David et G. Comings, Brenda, A controlled study of tourette syndrome. I. attention-deficit disorder, learning disorders, and school problems, American journal of human genetics , 41-II(5), 1987, pp. 701-741
A controlled study of tourette syndrome. II. conduct
Authors: Comings, David E. Comings, Brenda G.
Journal: American journal of human genetics
Citation: E. Comings, David et G. Comings, Brenda, A controlled study of tourette syndrome. II. conduct, American journal of human genetics , 41-II(5), 1987, pp. 742-760
A controlled study of tourette syndrome. III. phobias and panic attacks
Authors: Comings, David E. Comings, Brenda G.
Journal: American journal of human genetics
Citation: E. Comings, David et G. Comings, Brenda, A controlled study of tourette syndrome. III. phobias and panic attacks, American journal of human genetics , 41-II(5), 1987, pp. 761-781
A controlled study of tourette syndrome. IV. obsessions, compulsions, and schizoid behaviors
Authors: Comings, David E. Comings, Brenda G.
Journal: American journal of human genetics
Citation: E. Comings, David et G. Comings, Brenda, A controlled study of tourette syndrome. IV. obsessions, compulsions, and schizoid behaviors, American journal of human genetics , 41-II(5), 1987, pp. 782-803
A controlled study of tourette syndrome. V. depression and mania
Authors: Comings, David E. Comings, Brenda G.
Journal: American journal of human genetics
Citation: E. Comings, David et G. Comings, Brenda, A controlled study of tourette syndrome. V. depression and mania, American journal of human genetics , 41-II(5), 1987, pp. 804-821
A controlled study of tourette syndrome. VI. early development, sleep problems, allergies, and handedness
Authors: Comings, David E. Comings, Brenda G.
Journal: American journal of human genetics
Citation: E. Comings, David et G. Comings, Brenda, A controlled study of tourette syndrome. VI. early development, sleep problems, allergies, and handedness, American journal of human genetics , 41-II(5), 1987, pp. 822-838
A controlled study of tourette syndrome. VII. summary: A common genetic disorder causing disinhibition of the limbie system
Authors: Comings, David E.
Journal: American journal of human genetics
Citation: E. Comings, David, A controlled study of tourette syndrome. VII. summary: A common genetic disorder causing disinhibition of the limbie system, American journal of human genetics , 41-II(5), 1987, pp. 839-866
Development of a single probe for documentation of chimerism following bone marrow transplantation
Authors: Yam, Priscilla Petz, Lawrence D. Ali, Sher Stock, A. Dean Wallace, R. Bruce
Journal: American journal of human genetics
Citation: Yam, Priscilla et al., Development of a single probe for documentation of chimerism following bone marrow transplantation, American journal of human genetics , 41-II(5), 1987, pp. 867-881
Induction of sister chromatid exchanges at common fragile sites
Authors: Glover, Thomas W. Stein, Constance K.
Journal: American journal of human genetics
Citation: W. Glover, Thomas et K. Stein, Constance, Induction of sister chromatid exchanges at common fragile sites, American journal of human genetics , 41-II(5), 1987, pp. 882-890
DNA restriction-site polymorphisms associated with the alpha1-antitrypsin gene
Authors: Cox, Diane Wilson Billingsley, Gail D. Mansfield, Tammy
Journal: American journal of human genetics
Citation: Cox, Diane Wilson et al., DNA restriction-site polymorphisms associated with the alpha1-antitrypsin gene, American journal of human genetics , 41-II(5), 1987, pp. 891-906
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