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Общее количество найденных документов : 228
Показаны документы с 1 по 20
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1.
| Villaverde 3D gene of foot-and-mouth disease virus. Conservation by convergence of average sequences // J. Mol. Biol, 1988. Vol. 204, N 3.-С.771-776
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2.
| A deletion in the 5'-region of the neurofibromatosis type 1 (NF1) gene // Hum. Genet., 1994. Vol. 94, N 1.-С.97-100
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3.
| Rank A hierarchial analysis of genetic differentiation in a montane leaf beetle Chrysomela aeneicollis (Coleoptera: Chrysomelidae) // Evolution.. -USA, 1992. Vol. 46, N 4.-С.1097-1111
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4.
| A mendelian form of obsessive-compulsive disorder derived from symptom-based factors // Amer. J. Med. Genet., 1998. Vol. 81, N 6.-С.546
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5.
| A novel fusion gene, SSI8LI/SSXI, in synovial sarcoma // Genes, Chromosomes and Cancer, 2003. Vol. 37, N 2.-С.195-200
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| Susheela G. A study of population dynamics in Syphacia obvelata a nematode parasite of a bandicoot rat with reference to 'r' & 'k' selection // Riv. parassitol., 1989. Vol. 50, N 1-2.-С.245-255
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7.
| Absence of 717 APP mutation in Italian families with early onset familial Alzheimer's disease // Neurobiol. Aging, 1992. Vol. 13, Suppl. n 1.-С.71
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| Absence of extensive genetic heterogeneity of hepatitis C virus in antibody-negative chronic hepatitis C // J. Med. Virol., 1996. Vol. 49, N 2.-С.87-90
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9.
| Felbor Adult vitelliform macular dystrophy is frequently associated with mutations in the peripherin/RDS gene // Hum. Mutat., 1997. Vol. 10, N 4.-С.301-309
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| Aggiornamenti nella diagnosi della distrofia miotonica // G. neuropsicofarmacol., 2000. Vol. 22, N 6.-С.179-182
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| Cormier-Daire Allelic and nonallelic heterogeneity in dyschondrosteosis (Leri-Weill syndrome) // Amer. J. Med. Genet., 2001. Vol. 106, N 4.-С.272-274
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12.
| Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant // Hum. Mol. Genet., 1996. Vol. 5, N 7.-С.985-988
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13.
| An autosomal dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy, not linked to the sulfonylurea receptor locus // J. Clin. Endocrinol. and Metab., 1997. Vol. 82, N 4.-С.1192-1194
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14.
| An autosomal dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy, not linked to the sulfonylurea receptor locus // J. Clin. Endocrinol. and Metab., 1997. Vol. 82, N 4.-С.1192-1194
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15.
| Ruiz-Garcia Analisis de seis poblaciones latinoamericanas de gatos mediante genes del pelaje y marcadores microsatelites // Acta zool. mex., 2003, N 89.-С.261-286
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16.
| Ruiz-Garcia Analisis de seis poblaciones latinoamericanas de gatos mediante genes del pelaje y marcadores microsatelites // Acta zool. mex., 2003, N 89.-С.261-286
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17.
| Sanchez I. Analysis of genetic and antigent heterogenety in a dengue -2 population of mexican genotype // 8th Int. Congr. Immunol., Budapest, Aug. 23-28, 1992. -Budapest, 1992.-С.405
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18.
| Analysis of the genetic diversity and phylogenetic relationship of Italian isolates of feline immunodeficiency virus indicates a high prevalence and heterogeneity of subtype B // J. Gen. Virol., 1997. Vol. 78, N 9.-С.2245-2257
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19.
| Analysis of the genetic diversity and phylogenetic relationship of Italian isolates of feline immunodeficiency virus indicates a high prevalence and heterogeneity of subtype B // J. Gen. Virol., 1997. Vol. 78, N 9.-С.2245-2257
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20.
| Assessing genetic heterogeneity within bacterial species isolated from gastrointestinal and environmental samples: How many isolates does it take? // Appl. and Environ. Microbiol., 2008. Vol. 74, N 11.-С.3490-3496
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