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 25 limit 25" ACNP - Italian Periodicals Catalogue
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Articles table of contents

Results : 26-50/119
Huntington disease in maryland: clinical aspects of racial variation
Authors: Folstein, S.E. Chase, G.A. Wahl, W.E. McDonnell, A.M. Folstein, M.F.
Journal: American journal of human genetics
Citation: Folstein, S.e et al., Huntington disease in maryland: clinical aspects of racial variation, American journal of human genetics , 41-I(2), 1987, pp. 168-179
The use of map functions in multipoint mapping
Authors: Pascoe, L. Morton, N.E.
Journal: American journal of human genetics
Citation: L. Pascoe, et Morton, N.e, The use of map functions in multipoint mapping, American journal of human genetics , 40(2), 1987, pp. 174-183
Multipoint gene mapping using seriation. I. General methods
Authors: Buetow, K.H. Chakravarti, A.
Journal: American journal of human genetics
Citation: Buetow, K.h et A. Chakravarti,, Multipoint gene mapping using seriation. I. General methods, American journal of human genetics , 41-I(2), 1987, pp. 180-188
Multipoint gene mapping using seriation. II. Analysis of simulated and empirical data
Authors: Buetow, K.H. Chakravarti, A.
Journal: American journal of human genetics
Citation: Buetow, K.h et A. Chakravarti,, Multipoint gene mapping using seriation. II. Analysis of simulated and empirical data, American journal of human genetics , 41-I(2), 1987, pp. 189-201
Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor
Authors: Dao, D.D. Schroeder, W.T. Chao, L.-Y. Kikuchi, H. Strong, L.C. Riccardi, V.M. Pathak, S. Nichols, W.W. Lewis, W.H. Saunders, G.F.
Journal: American journal of human genetics
Citation: Dao, D.d et al., Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor, American journal of human genetics , 41-I(2), 1987, pp. 202-217
Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions
Authors: Francke, U. Harper, J.F. Darras, B.T. Cowan, J.M. McCabe, E.R.B. Kohlschutter, A. Seltzer, W.K.
Journal: American journal of human genetics
Citation: U. Francke, et al., Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions, American journal of human genetics , 40(3), 1987, pp. 212-227
Spontaneous mutation and parental age in humans
Authors: Risch, N. Reich, E.W. Wishnick, M.M. McCarthy, J.G.
Journal: American journal of human genetics
Citation: N. Risch, et al., Spontaneous mutation and parental age in humans, American journal of human genetics , 41-I(2), 1987, pp. 218-248
Mapping of DNA markers linked to the cystic fibrosis locus on the long arm of chromosome
Authors: Zengerling, S. Tsui, L.C. Grzeschik, K. Olek, K. Riordan, J.R.
Journal: American journal of human genetics
Citation: S. Zengerling, et al., Mapping of DNA markers linked to the cystic fibrosis locus on the long arm of chromosome, American journal of human genetics , 40(3), 1987, pp. 228-236
A combined segregation and linkage analysis of insulin-dependent diabetes mellitus
Authors: Rich, S.S. Green, A. Morton, N.E. Barbosa, J.
Journal: American journal of human genetics
Citation: Rich, S.s et al., A combined segregation and linkage analysis of insulin-dependent diabetes mellitus, American journal of human genetics , 40(3), 1987, pp. 237-249
Complex segregation analysis of febrile convulsions
Authors: Rich, S.S. Annegers, J.F. Hauser, W.A. Anderson, V.E.
Journal: American journal of human genetics
Citation: Rich, S.s et al., Complex segregation analysis of febrile convulsions, American journal of human genetics , 41-I(2), 1987, pp. 249-257
An algorithm for automatic genotype elimination
Authors: Lange, K. Goradia, T.M.
Journal: American journal of human genetics
Citation: K. Lange, et Goradia, T.m, An algorithm for automatic genotype elimination, American journal of human genetics , 40(3), 1987, pp. 250-256
Deficient fumarase activity in an infant with fumaricacidemia and its distribution between the different forms of the enzyme seen on isoelectric focusing
Authors: Petrova-Benedict, R. Robinson, B.H. Stacey, T.E. Mistry, J. Chalmers, R.A.
Journal: American journal of human genetics
Citation: R. Petrova-benedict, et al., Deficient fumarase activity in an infant with fumaricacidemia and its distribution between the different forms of the enzyme seen on isoelectric focusing, American journal of human genetics , 40(3), 1987, pp. 257-266
Formulas for mean restriction-fragment lenghts and related quantities
Authors: Biggins, J.D. Cannings, C.
Journal: American journal of human genetics
Citation: Biggins, J.d et C. Cannings,, Formulas for mean restriction-fragment lenghts and related quantities, American journal of human genetics , 41-I(2), 1987, pp. 258-265
An improved method for heterozygote detection of cystinosis, using polymorphonuclear leukocytes
Authors: Smolin, L.A. Clark, K.F. Schneider, J.A.
Journal: American journal of human genetics
Citation: Smolin, L.a et al., An improved method for heterozygote detection of cystinosis, using polymorphonuclear leukocytes, American journal of human genetics , 41-I(2), 1987, pp. 266-275
Does the PI Polymorphism alone control alpha-1-antitrypsin expression?
Authors: Martin, N.G. Clark, P. Ofulue, A.F. Eaves, L.J. Corey, L.A. Nance, W.E.
Journal: American journal of human genetics
Citation: Martin, N.g et al., Does the PI Polymorphism alone control alpha-1-antitrypsin expression?, American journal of human genetics , 40(3), 1987, pp. 267-277
Laurence hasbrouck snyder: pioneer in human genetics
Authors: Green, E.L.
Journal: American journal of human genetics
Citation: Green, E.l, Laurence hasbrouck snyder: pioneer in human genetics, American journal of human genetics , 41-I(2), 1987, pp. 276-285
Human Albumin Genetic Variants: an attempt at a classification of european allotypes
Authors: Fine, J.M. Marneux, M. Rochu, D.
Journal: American journal of human genetics
Citation: Fine, J.m et al., Human Albumin Genetic Variants: an attempt at a classification of european allotypes, American journal of human genetics , 40(3), 1987, pp. 278-286
Multipoint linkage analysis of loci in the proximal long arm of the human x chromosome: application to mapping the choroideremia locus
Authors: Lesko, J.G. Lewis, R.A. Nussbaum, R.L.
Journal: American journal of human genetics
Citation: Lesko, J.g et al., Multipoint linkage analysis of loci in the proximal long arm of the human x chromosome: application to mapping the choroideremia locus, American journal of human genetics , 40(4), 1987, pp. 303-311
Efficient isolation of x chromosome-specific single-copy probes from a cosmid library of a human x/hamster hybrid-cell line:mapping of new probes close to the locus for x-linked mental retardation
Authors: Hofker, M.H. Bergen, A.A.B. Skraastad, M.I. Carpenter, N.J. Veenema, H. Connor, J.M.
Journal: American journal of human genetics
Citation: Hofker, M.h et al., Efficient isolation of x chromosome-specific single-copy probes from a cosmid library of a human x/hamster hybrid-cell line:mapping of new probes close to the locus for x-linked mental retardation, American journal of human genetics , 40(4), 1987, pp. 312-328
An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13
Authors: Farrer, L.A. Goodfellow, P.J. Lamarche, C.M. Franjkovic, I. Myers, S. White, B.N. Holden, J.J.A. Kidd, J.R. Simpson, N.E. Kidd, K.K.
Journal: American journal of human genetics
Citation: Farrer, L.a et al., An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13, American journal of human genetics , 40(4), 1987, pp. 329-337
Analisys of genetic interrelationship among HLA-associated diseases
Authors: Payami, Haydeh Khan, Muhammad A. Grennan, David M. Sanders, Paul A. Dyer, Philip A. Thomson, Glenys
Journal: American journal of human genetics
Citation: Payami, Haydeh et al., Analisys of genetic interrelationship among HLA-associated diseases, American journal of human genetics , 41-I(2), 1987, pp. 331-349
Linkage disequilibrium of plasminogen polymorphisms and assignment of the gene to human chromosome 6q26-6q27
Authors: Murray, J.C. Buetow, K.H. Donovan, M. Hornung, S. Motulsky, A.G. Disteche, C. Dyer, K. Swisshelm, K. Anderson, J. Giblett, E. Sadler, E. Eddy, R. Shows, T.B.
Journal: American journal of human genetics
Citation: Murray, J.c et al., Linkage disequilibrium of plasminogen polymorphisms and assignment of the gene to human chromosome 6q26-6q27, American journal of human genetics , 40(4), 1987, pp. 338-350
DSLINK: A computer program for Gene-centromere linkage analysis in families with a trisomic offspring
Authors: Halloran, Susan L. Chakravarti, Aravinda
Journal: American journal of human genetics
Citation: L. Halloran, Susan et Chakravarti, Aravinda, DSLINK: A computer program for Gene-centromere linkage analysis in families with a trisomic offspring, American journal of human genetics , 41-I(3), 1987, pp. 350-355
The polymorphic locus for glycogen storage disease VI (liver glycogen phosphorylase) maps to chromosome 14
Authors: Newgard, C.B. Fletterick, R.J. Anderson, L.A. Lebo, R.V.
Journal: American journal of human genetics
Citation: Newgard, C.b et al., The polymorphic locus for glycogen storage disease VI (liver glycogen phosphorylase) maps to chromosome 14, American journal of human genetics , 40(4), 1987, pp. 351-364
A deductive method of haplotype analysis in pedigrees
Authors: Wijsman, Ellen M.
Journal: American journal of human genetics
Citation: M. Wijsman, Ellen, A deductive method of haplotype analysis in pedigrees, American journal of human genetics , 41-I(3), 1987, pp. 356-373
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