Поисковый запрос: (<.>S=ХРОМОСОМА 20<.>) |
Общее количество найденных документов : 35
Показаны документы с 1 по 20
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1.
| 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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2.
| True fetal mosaicism of an isochromosome of the long arm of a chromosome 20: The dilemma persists // Prenat. Diagn., 1997. Vol. 17, N 12.-С.1171-1175
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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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4.
| The neuronal nicotinic acetylcholine receptor in some hereditary epilepsies // Neurochem. Res., 2000. Vol. 25, N 5.-С.583-590
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5.
| 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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| The human TDE gene homologue: Localization to 20q13.1-13.3 and variable expression in human tumor cell lines and tissue // Mol. Carcinogenes., 1999. Vol. 26, N 3.-С.189-200
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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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| Refinement of the commonly deleted segment in myeloid leukemias with a del(20q) // Genes, Chromosomes and Cancer, 1998. Vol. 21, N 2.-С.75-81
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9.
| Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene // Nature Genet., 2000. Vol. 25, N 2.-С.144-146
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| Prenatally detected trisomy 20 mosaicism // Prenat. Diagn., 2005. Vol. 25, N 3.-С.239-244
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11.
| New susceptibility locus for NIDDM is localized to human chromosome 20q // Diabetes, 1997. Vol. 46, N 5.-С.876-881
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| Thakker R.V. Molecular genetics of endocrine tumours // J. Endocrinol., 1993. Vol. 137, Suppl..-С.11
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13.
| Nitsch Roger M. Methods of diagnosing or prognosing Alzheimer's disease
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14.
| Nitsch Roger M. Methods of diagnosing or prognosing Alzheimer's disease
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15.
| Nitsch Roger M. Methods of diagnosing or prognosing Alzheimer's disease
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16.
| Mechanismen und molekulare Grundlagen von Erbkrankheiten // Bioengineering, 1988. Vol. 4, N 4.-С.74-76
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17.
| 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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18.
| Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy // Diabetes, 1997. Vol. 46, N 5.-С.882-886
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19.
| 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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20.
| Jagged1 mutations in patients ascertained with isolated congenital heart defects // Amer. J. Med. Genet., 1999. Vol. 84, N 1.-С.56-60
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