Поисковый запрос: (<.>S=ХРОМОСОМА 20<.>) |
Общее количество найденных документов : 35
Показаны документы с 1 по 20
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1.
| Nitsch Roger M. Methods of diagnosing or prognosing Alzheimer's disease
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| Nitsch Roger M. Methods of diagnosing or prognosing Alzheimer's disease
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| Pinkel Array-based detection of genetic alterations associated with disease
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| Nitsch Roger M. Methods of diagnosing or prognosing Alzheimer's disease
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| Ten polymorphic DNA loci, including five in the rat MHC (RT1) region, form a single linkage group on rat chromosome 20 // Immunogenetics, 1995. Vol. 41, N 5.-С.316-319
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| Nath Swapan K. Two-trait-locus linkage analyses of asthma susceptibility // Genet. Epidemiol., 2001. Vol. 21, прил. N 1.-С.278-283
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| Steinlein O.K. Le KCNQ2 est le premier gene pour lequel une mutation est demontree chez des patients souffrant d'epilepsie generalisee idiopathique // Pathol. Biol., 1998. Vol. 46, N 9.-С.683-684
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| The neuronal nicotinic acetylcholine receptor in some hereditary epilepsies // Neurochem. Res., 2000. Vol. 25, N 5.-С.583-590
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| Genetic linkage of childhood atopic dermatitis to psoriasis susceptibility loci // Nature Genet., 2001. Vol. 27, N 4.-С.372-373
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| Genetic linkage of childhood atopic dermatitis to psoriasis susceptibility loci // Nature Genet., 2001. Vol. 27, N 4.-С.372-373
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| Genetic linkage of childhood atopic dermatitis to psoriasis susceptibility loci // Nature Genet., 2001. Vol. 27, N 4.-С.372-373
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| Constitutional deletion of chromosome 20q in two patients affected with Albright hereditary osteodystrophy // Amer. J. Med. Genet., 2002. Vol. 113, N 2.-С.167-172
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| The paradox of 20q11.21 amplification in a subset of cases of myeloid malignancy with chromosome 20 deletion // Genes, Chromosomes and Cancer, 2010. Vol. 49, N 11.-С.998-1013
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| Mechanismen und molekulare Grundlagen von Erbkrankheiten // Bioengineering, 1988. Vol. 4, N 4.-С.74-76
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| Thakker R.V. Molecular genetics of endocrine tumours // J. Endocrinol., 1993. Vol. 137, Suppl..-С.11
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| Linkage studies for T2D in chop and C/EBPbeta chromosomal regions in Italians // J. Cell. Physiol., 2007. Vol. 213, N 2.-С.552-555
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| Imprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in human myeloid malignancies // Proc. Nat. Acad. Sci. USA, 2004. Vol. 101, N 19.-С.7341-7346
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| The human transcription factor activation protein-2 gamma (AP-2'гамма'): Gene structure, promoter, and expression in mammary carcinoma cell lines // Gene, 2002. Vol. 301, N 1-2.-С.43-51
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| Prenatally detected trisomy 20 mosaicism // Prenat. Diagn., 2005. Vol. 25, N 3.-С.239-244
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20.
| Genome-wide scan and schizophrenia in African Americans // Amer. J. Med. Genet., 1998. Vol. 81, N 6.-С.454-455
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